반응식
C1CCCCC1.C([O:30][CH:31]([C:33]1[CH:38]=[CH:37][CH:36]=[CH:35][C:34]=1[Br:39])[CH3:32])(=O)CCCCCCCCCCCCCCCCCCCCC>O>[Br:39][C:34]1[CH:35]=[CH:36][CH:37]=[CH:38][C:33]=1[C@@H:31]([OH:30])[CH3:32]참가 물질
실험 절차
Interesterification was carried out by using 5 g of Lipase P of Pseudomonas fluorescens origin (a product of Amano Pharmaceutical Co., Ltd.), 10 g of (R,S)-1-2-(bromophenyl)ethanol, 30 g of tribehen and 450 ml of cyclohexane at 50° C. for 72 hours in the same manner as in Example 8. The water content of the reaction system was 0.01% by weight, and 90% of the lipase particles had a particle size of 30 to 50 μm. Gas chromatography of the reaction mixture revealed that 48 mol % of (R,S)-1-(2-bromophenyl)ethanol had been converted to 1-(2-bromophenyl)ethyl behenate. The reaction mixture was treated in the same manner as in Example 8, and the residue was subjected to simple distillation at 110° C. and 5 mmHg to recover unreacted (S)-(-)-1-(2-bromophenyl)ethanol (yield: 82%; chemical purity: 99.9%; optical purity: 98% ee).
후처리
- additionThe reaction mixture was treated in the same manner as in Example 8
- distillationthe residue was subjected to simple distillation at 110° C.
출처 및 근거
- ORD 기록
- ord-34c2dfe66184439aa444fd21605461f1
- 출처 데이터셋
- uspto-grants-1997_12
- 특허 번호
- US05696299
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