Claims
- 1. A process for the preparation of oxalyl chloride comprising:
- (i) esterifying ethylene glycol with trichloroacetyl chloride, in the absence of any reaction solvent other than trichloroacetyl chloride, to afford ethylene glycol bis-trichloroacetate, the reaction mixture for the esterification consisting essentially of ethylene glycol, trichloroacetyl chloride and the reaction products thereof, and the hydrochloric acid produced during the esterification being removed from the reaction mixture by distillation;
- (ii) photochemically chlorinating the resulting ethylene glycol bis-trichloroacetate, at a temperature of from about 50.degree. to 200.degree. C., to afford tetrachloroethylene glycol bis-trichloroacetate;
- (iii) decomposing the resulting tetrachloroethylene glycol bis-trichloroacetate, at a temperature of from about 50.degree. to 160.degree. C., in the presence of trichloroacetyl chloride as the sole reaction solvent, and in the presence of a decomposition catalyst, to afford oxalyl chloride and trichloroacetyl chloride; and
- (iv) separating the resulting oxalyl chloride.
- 2. The process as defined by claim 1, the chlorination step (ii) being conducted at a temperature of from about 80.degree. to 160.degree. C.
- 3. The process as defined by claim 1, the reaction medium containing no more than about 1 ppm metallic salts.
- 4. The process as defined by claim 1, the esterification step (i) being conducted with an about 2 to 500% by weight stoichiometric excess of trichloroacetyl chloride, and at a temperature gradually increasing from 60.degree. to 80.degree. C. to reflux.
- 5. The process as defined by claim 1, the chlorination step (ii) being conducted in the presence of a 1 to 5% stoichiometric excess of chlorine, and under a pressure of from about 500 nm Hg, absolute, to 5 bars.
- 6. The process as defined by claim 1, the decomposition catalyst being a tertiary amine, or chlorhydrate thereof, in an amount of from 20 to 250 ppm.
- 7. The process as defined by claim 6, the decomposition step (iii) being conducted at a temperature of from 60.degree. to 120.degree. C.
- 8. The process as defined by claim 6, the decomposition catalyst being selected from the group comprising triethylamine, pyridine and dimethylaniline.
- 9. The process as defined by claim 1, all of the steps (i), (ii) and (iii) being conducted in the same reaction vessel.
- 10. The process as defined by claim 1, the chlorination step (ii) being conducted in a reaction vessel separate from that in which the steps (i) and (iii) are conducted.
- 11. The process as defined by claim 9, said reaction vessel being comprised of a member selected from the group comprising glass, steel, and polymer devoid of metallic filler.
- 12. The process as defined by claim 10, said reaction vessels each being comprised of a member selected from the group comprising glass, steel, and polymer devoid of metallic filler.
- 13. The process as defined by claim 1, wherein step (ii) is conducted in the absence of any reaction solvent.
- 14. The process as defined by claim 1, wherein step (ii) is conducted in the presence of trichloroacetyl chloride as the sole reaction solvent.
Priority Claims (1)
Number |
Date |
Country |
Kind |
78 07740 |
Mar 1978 |
FRX |
|
CROSS-REFERENCE TO RELATED APPLICATION
This is a continuation of our copending, commonly assigned application, Ser. No. 22,055, filed Mar. 19, 1979 and now abandoned.
US Referenced Citations (1)
Number |
Name |
Date |
Kind |
2816140 |
Ellingboe et al. |
Dec 1957 |
|
Non-Patent Literature Citations (1)
Entry |
Scattergood et al., J.A.C.S., vol. 72 (1950). |
Continuations (1)
|
Number |
Date |
Country |
Parent |
22055 |
Mar 1979 |
|