Preparation of methylene-bridged hetero compounds and novel bis (diorganophosphino) methanes

Abstract

Preparation of methylene-bridged compounds of the formula I ##STR1## where R.sup.1 to R.sup.4 are identical or different and are each saturated C.sub.1 -C.sub.30 -hydrocarbyl, unsubstituted phenyl, phenyl substituted by substituents inert under the reaction conditions, or hydrogen, E.sup.1 and E.sup.2 are identical or different and are each phosphorus, arsenic or antimony, and X is a chemical bond or oxygen by reacting a tin compound of the general formula IIR.sub.3.sup.5 Sn--CH.sub.2 M, IIwhere R.sup.5 is C.sub.1 --C.sub.20 -hydrocarbyl and M is an alkali metal, with a compound of the general formula III ##STR2## where Y is halogen, metallating the thus-obtained tin compound of the general formula IV ##STR3## with an alkali organometallic, and reacting the product with a compound of the general formula V ##STR4## to give a methylene-bridged compound of the formula I. And novel bis(diorganophosphino)methanes.

Description

BACKGROUND OF THE INVENTION

1. The present invention relates to a novel process for the preparation of methylene-bridged bisheteroatom compounds having heteroatoms of group 15 of the Periodic Table.

This invention further relates to novel bis(diorganophosphino)methanes.

2. Description of the Related Art

Bis(dialkylphosphino)alkanes and bis(diarylphosphino)alkanes represent an important group of ligands in organometallic chemistry and are of interest especially for organometallic catalysts. For instance, bis(diorganophosphino)methanes and metal compounds can be reacted to prepare four-membered ring chelates having small phosphorus-metal-phosphorus angles. Such compounds, especially those containing the metals cobalt, rhodium, iridium, nickel, palladium and platinum in the oxidation states of 0 to 3, are compounds sought after for use as catalysts and as intermediates of catalytic cycles. The compounds sought after serve as ligands for transition metals for homogeneous catalysts in hydrogenations, hydroformylations, carbonylations and in the oligomerization and cooligomerization of unsaturated compounds.

However, bis(diphosphino)methanes tend to form two-or multi-center complexes instead of the four-membered, metal-containing rings desired. Therefore, the stabilization of mononuclear four-membered ring chelate complexes requires tailor-made bis(diphosphino)methanes having specific steric and electronic properties in order that polynuclear structures may be destabilized.

Wide industrial use of bis(diorganophosphino)methanes was up to now prevented by the difficult accessibility of these compounds. Thus, Karsch (Z. Naturforsch. 38b (1983) 1027) describes the synthesis of bis(di-tert.-butylphosphino)methane in unsatisfactory yields from bis(dichlorophosphino)methane and tert.-butyllithium.

DE-A 41 34 772 teaches that better yields are obtained when di-tert.-butyl-chlorophosphane is reacted with a metallated di-tert.-butylphosphinomethane. A problem, however, is the formation of tetraorganobisphosphanes, which is observed especially with other sterically demanding ligands on the phosphorus, since these compounds are difficult to separate from the desired products.

It is an object of the present invention to make available a process allowing the preparation of bis(diorganophosphino)methanes in good yields. Also to be prepared are bis(diorganophosphino)methanes having sterically demanding ligands, ligands having optically active centers being especially sought after because of the special catalytic properties associated with this property. Finally, novel bis(diorganophosphino)methanes are to be made available.

SUMMARY OF THE INVENTION

We have found that this object is achieved by a process for the preparation of methylene-bridged compounds of the formula I ##STR5## where R.sup.1 to R.sup.4 are identical or different and are each saturated C.sub.1 -C.sub.30 -hydrocarbyl, unsubstituted phenyl, phenyl-substituted by substituents inert under the reaction conditions, or hydrogen, E.sup.1 and E.sup.2 are identical or different and are each phosphorus, arsenic or antimony, and X is a chemical bond or oxygen, which comprises reacting a tin compound of the formula II

R.sub.3.sup.5 Sn--CH.sub.2 M II, where R.sup.5 is C.sub.1 -C.sub.20 -hydrocarbyl and M is an alkali metal, with a compound of the formula III ##STR6## where Y is halogen, metallating the thus-obtained tin compound of the formula IV ##STR7## with an alkali organometallic, and reacting the product with a compound of the formula V ##STR8## to give a methylene-bridged compound of the formula I.

This invention also provides novel bis(diorganophosphino)methanes.

The process according to the invention makes possible the preparation of compounds of the formula I. The substituents have the following meanings:

R.sup.1 -R.sup.4 : saturated C.sub.1 -C.sub.30 -hydrocarbon radicals, preferably C.sub.4 -C.sub.14 radicals such as tert.-butyl, tert.-amyl and 2-ethyl-hexyl; especially preferred are radicals carrying a tertiary carbon in a position beta to the heteroatom E.sup.1 or E.sup.2, such as menthyl, longifolyl, alpha-pinyl, beta-pinyl, 3-caryl and 2-caryl; also suitable are phenyl radicals, which may carry one to five substituents inert under the reaction conditions; E.sup.1, E.sup.2 : phosphorus, arsenic, antimony, preferably phosphorus; the radicals are preferably identical; X: a chemical bond or oxygen, preferably a chemical bond.

The compounds of the formula I are obtainable by a multi-step process. As starting material there may be used a metallated tin compound of the formula II, where the radicals have the abovementioned meanings. R.sup.5 is preferably phenyl or methyl, M is preferably lithium or sodium. The compounds of the formula II are obtainable in a conventional manner by reacting the appropriate halostannanes, especially the iodostannanes, with alkali organometallics such as butyllithium or methyllithium. The compounds of the formula II are reacted with a heteroatom compound of the formula III. These compounds carry a halogen such as fluorine, chlorine, bromine or iodine, preferably chlorine. They are obtainable in a manner known per se, for example by reacting halogen compounds of phosphorus, arsenic or antimony with metallated hydrocarbons with elimination of metal halide. The compounds of the formulae II and III are preferably reacted in stoichiometric amounts. In a preferred embodiment, the reaction is carried out in an inert solvent such as toluene, hexane or mixtures thereof. The starting materials are reacted in the cold, for example at from -70.degree. to -20.degree. C. After the reaction has ended, the corresponding compound of the formula IV can be isolated by known methods, for example extraction of the alkali metal halide formed with water, drying of the organic phase and crystallization, if necessary after a change of solvent.

The compound thus obtained of the formula IV is reacted with an alkali organometallic. Phenyllithiumis preferred, but compounds such as butyllithium and methyllithium are also suitable. Stoichiometric amounts of the alkali organometallic are preferred. Excesses may be used, but they have to be destroyed prior to any further reaction. Especially preferred is the elimination of tetraphenyltin from compound IV, because the former crystallizes easily and can thus be easily removed from the reaction mixture. To the reaction mixture is then added a compound of the formula V, which is obtainable analogously to compounds of the formula III. For this reaction as well, a stoichiometric reaction of the starting materials is preferred. In a preferred embodiment, the compound of the formula V is added to the reaction mixture at temperatures of from -70.degree. to -20.degree. C. After extraction with water, the product is isolated by crystallization from the organic phase.

Specific compounds I are preferably bis(dimenthylphosphino)methane, furthermore bis(di-tert.-butyl-phosphino)methane, (dimenthylphosphino)(diphenylphosphino)-methane, (dimenthylphosphino)(di-tert.-butylphosphino)methane and (di-tert.-butylphosphino)(diphenylphosphino)methane and compounds where R.sup.1 and R.sup.2 are each menthyl and R.sup.3 and R.sup.4 are each phenyl or C.sub.4 -C.sub.14 -hydrocarbon radicals, having in a position beta to E.sup.2 a tertiary carbon.

The process according to the invention makes possible the preparation of much sought-after methylene-bridged heteroatom compounds of group 15 of the Periodic Table in high yields.

EXAMPLES

a) Preparation of (men).sub.2 P--CH.sub.2 --SnPh.sub.3 (men=menthyl)

Menthyl is the radical ##STR9## (men).sub.2 PCl+LiCH.sub.2 --SnPh.sub.3 .fwdarw.(men).sub.2 P--CH.sub.2 --SnPh.sub.3 +LiCl

To a solution of 21.27 g (43.32 mmol) of ICH.sub.2 --SnPh.sub.3 in 200 ml of toluene was added dropwise at -55.degree. C. within 30 min 16.05 ml of a 2.7 M solution of butyllithium (43.32 mmol) in hexane. The mixture was stirred for 30 min, at which point, again at -55.degree. C., a solution of 14.94 g (43.32 mmol) of (men).sub.2 PCl in 60 ml of toluene were slowly added. The reaction solution was then carefully warmed, stirred for 2 h at -15.degree. C. and for 1 h at room temperature, and cooled to 0.degree. C., at which point 50 ml of H.sub.2 O were added. The phases were then separated, the organic phase was washed two times with 50 ml H.sub.2 O each time and dried by stirring for 5 min over Na.sub.2 SO.sub.4. After filtration, the solvent was distilled off under reduced pressure, the residue was extracted with 200 ml of warm pentane, and the solution was concentrated by boiling until crystallization set in, and then slowly cooled to -18.degree. C. A colorless, fluffy precipitate sensitive to hydrolysis was formed, which was filtered off and dried under reduced pressure. Concentrating the mother liquor to about 30 ml and cooling to -18.degree. C. afforded more product.

Yield: 20.16 g (69%)

Melting point: 120-121.degree. C.

.sup.13 C-NMR (C.sub.6 D.sub.6): .delta.139.54 (d,J(PC)=1.8,J(.sup.117/119 SnC)=485.6 Hz, ipso-C of C.sub.6 H.sub.5), 137.59 (d,J(PC)=1.3,J(.sup.117/119 SnC)=35.9 Hz, ortho-C of C.sub.6 H.sub.5), 129.20 (s,para-C of C.sub.6 H.sub.5), 128.79 (s,J(.sup.117/119 SnC)=50.1 Hz, meta-C of C.sub.6 H.sub.5), 45.82 (d,J(PC)=19.2 Hz, CH of men), 44.76 (d,J(PC)=9.4 Hz, CH of men), 40.20 (d,J(PC)=19.1 Hz, CH of men), 39.11 (s, CH.sub.2 of men), 36.28 (s, CH.sub.2 of men), 35.33 (s, CH.sub.3 of men), 35.22 (s, CH.sub.2 of men, 33.91 (s,CH of men), 33.69 (d,J(PC)=23.8 Hz, CH of men), 33.66 (s, CH of men), 28.07 (s, CH of men), 27.60 (d,J(PC) 6.4 Hz, CH of men), 26.13 (d,J(PC)=8.4 Hz, CH.sub.2 of men), 25.52 (d,J(PC)=6.3 Hz, CH.sub.2 of men), 23.22, 22.98, 22.19, 21.97, 16.10, 15.67, (all s, CH.sub.3), 0.46 (d,J(PC)=45.6 Hz, P-CH.sub.2).

.sup.31 P-NMR (C.sub.6 D.sub.6): .delta.-31.87 (s,J(.sup.117/119 SnP)=115.5 Hz)

b) Preparation of (men).sub.2 P--CH.sub.2 --P(men).sub.2 ##STR10##

To a solution of 13.20 g (19.60 mmol) of (men).sub.2 P--CH.sub.2 --SnPh.sub.3 in 200 ml of Et.sub.2 O was added at 20.degree. C. within 30 min 11.04 ml of a 1.73 M solution of phenyllithium (19.10 mmol) in diethyl ether/cyclohexane (30:70), and the mixture was stirred for 45 min. After only a few minutes, SnPh.sub.4 began to precipitate as a colorless solid. The reaction mixture was then cooled to -25.degree. C., and a solution of 6.59 g (19.10 mmol) of (men).sub.2 PCl in 100 ml of Et.sub.2 O was added dropwise within 45 min. Stirring was continued for a further 60 min at -25.degree. C., the cooling bath was removed and the solvent was distilled off under reduced pressure as soon as the mixture had reached room temperature. The residue was extracted with 250 ml of pentane, and 50 ml of H.sub.2 O were added to the extract. The phases were then separated, and the organic phase washed two times with 50 ml of H.sub.2 O each time and dried over Na.sub.2 SO.sub.4. After filtration, the solvent was distilled off under reduced pressure and the residue was recrystallized from 170 ml of propanol. A colorless, air-sensitive solid was obtained.

Yield: 7.84 g (65%)

Melting point 161-163.degree. C.

.sup.13 C-NMR (C.sub.6 D.sub.6): .delta.46.79 (vt,N=20.5 Hz,CH), 44.84 (vt,N=11.2 Hz,CH), 40.45 (s, CH.sub.2 of men), 40.11 (vt,N=9.8 Hz,CH), 36.82 (s, CH.sub.2 of men), 35.43 (s, CH.sub.2 of men), 35.34 (s,CH.sub.2 of men), 34.24 (s, 2.times. CH), 33.07 (vt,N=22.7 Hz,CH), 28.00 (vt,N=22.3 Hz,CH), 27.70 (vt,N=26,1 Hz,CH), 26.28 (vt,N=7.9 Hz,CH.sub.2 of men), 25.56 (vt,N=6.1 Hz,CH.sub.2 of men), 23.19, 23.00, 22.39, 21.78, 15.72, 15.56 (all s, CH.sub.3), 11.80 (t,J(PC)=28.5 Hz), P--CH.sub.2 --P). v is a virtual spin system.

.sup.31 P-NMR (C.sub.6 D.sub.6): .delta.-36.73 (s).

Claims

1. A process for the preparation of methylene-bridged compounds of the formula I ##STR11## where R.sup.1 to R.sup.4 are identical or different and are each saturated C.sub.1 -C.sub.30 -hydrocarbyl, unsubstituted phenyl, phenyl substituted by substituents inert under the reaction conditions, or hydrogen, E.sup.1 and E.sup.2 are identical or different and are each phosphorus, arsenic or antimony, and X is a chemical bond or oxygen, which comprises reacting a tin compound of the general formula II

R.sub.3.sup.5 Sn --CH.sub.2 M II,

where R.sup.5 is C.sub.1 -C.sub.20 -hydrocarbyl and M is an alkali metal, with a compound of the general formula III ##STR12## where Y is halogen, metallating the thus-obtained tin compound of the general formula IV ##STR13## with an alkali organometallic, and reacting the product with a compound of the general formula V ##STR14## to give a methylene-bridged compound of the formula I.

2. A process as defined in claim 1, wherein E.sup.1 and E.sup.2 are each phosphorus.

3. A process as defined in claim 1, wherein R.sup.1 to R.sup.4 are each saturated C.sub.4 -C.sub.14 -hydrocarbyl.

4. A process as defined in claim 1, wherein at least one of the radicals R.sup.1 to R.sup.4 has a tertiary carbon beta to E.sup.1 or E.sup.2.

5. A process as defined in claim 1, wherein R.sup.5 is phenyl.

6. A process as defined i claim 1, wherein R.sup.1 and R.sup.2 are each menthyl and R.sup.3 and R.sup.4 are each phenyl or saturated C.sub.4 -C.sub.14 -hydrocarbonyl having a tertiary carbon beta to E.sup.2.

7. A process as defined in claim 2, wherein R.sup.1 to R.sup.4 are each saturated C.sub.4 -C.sub.14 -hydrocarbyl.

8. A process as defined in claim 2, wherein at least one of the radicals R.sup.1 to R.sup.4 has a tertiary Carbon beta to E.sup.1 or E.sup.2.

9. A process as defined in claim 2, wherein R.sup.5 is phenyl.

10. A process as defined in claim 2, wherein R.sup.1 and R.sup.2 are each menthyl and R.sup.3 and R.sup.4 are each phenyl or saturated C.sub.4 -C.sub.14 -hydrocarbonyl having a tertiary carbon beta to E.sup.2.