Claims
- 1. Process for recovering an .alpha.-aminoalcohol by extraction from an aqueous solution comprising the following steps: at elevated pH an aromatic aldehyde is added to an aqueous solution of an aminoalcohol, the resulting mixture is converted with formation of the Schiff base of the aldehyde and the aminoalcohol, the resulting aqueous solution is extracted using a water-immiscible organic solvent, upon which the Schiff base in the resulting extract is hydrolized and the .alpha.-aminoalcohol or a salt thereof is recovered.
- 2. Process according to claim 1, characterized in that the aromatic aldehyde is added at a pH higher than 9.5.
- 3. The process of claim 2 wherein said pH is between 10.5 and 13.
- 4. Process according to claim 1, characterized in that the mixture of the aqueous solution of the aminoalcohol and the aromatic aldehyde is converted for at least 10 minutes.
- 5. The process of claim 4 wherein said conversion is for 10 to 120 minutes.
- 6. Process according to claim 4, characterized in that the mixture of the aqueous solution of the aminoalcohol and the aromatic aldehyde is converted for 20 to 80 minutes.
- 7. Process according to claim 1, characterized in that the stirring is carried out at a temperature of 0.degree.-100.degree. C.
- 8. The process according to claim 7 wherein said temperature is 40.degree.-60.degree. C.
- 9. Process according to claim 1, characterized in that the aldehyde is used in at least an equimolar amount in respect of the aminoalcohol.
- 10. Process according to claim 9, characterized in that a small excess of the aromatic aldehyde is applied in respect of the aminoalcohol.
- 11. Process according to claim 1, characterized in that the water-immiscible organic solvent is an ester.
- 12. Process according to claim 1, characterized in that the aromatic aldehyde is benzaldehyde.
- 13. Process for recovering an .alpha.-aminoalcohol by extraction from an aqueous solution, comprising the following steps: at elevated pH an aromatic aldehyde is added to an aqueous solution of an aminoalcohol, said aldehyde being used in at least an equimolar amount with respect to the aminoalcohol; the resulting mixture is converted with formation of the Schiff base of the aldehyde and the aminoalcohol; and the resulting aqueous solution is extracted using a water-immiscible organic solvent, upon which the Schiff base in the resulting extract is hydrolized and the .alpha.-aminoalcohol or a salt thereof is recovered.
Priority Claims (1)
Number |
Date |
Country |
Kind |
8703159 |
Dec 1987 |
NLX |
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Parent Case Info
This is a continuation of application Ser. No. 07/290,357, filed on Dec. 27, 1988, which was abandoned upon the filing hereof.
US Referenced Citations (1)
Number |
Name |
Date |
Kind |
4172846 |
Boesten |
Oct 1979 |
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Non-Patent Literature Citations (1)
Entry |
Evans et al., "Asymmetric Glycine Enolate Aldol Reactions: Synthesis of Cyclosporine's Unusual Amino Acid, MeBmt.sup.1," J. Am. Chem. Soc. 108:6757-61 (1986). |
Continuations (1)
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Number |
Date |
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Parent |
290357 |
Dec 1988 |
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