Diisopropyl Ether → (R)-2-bromo-1-(3-chlorophenyl)ethanol

HRID 357726

반응식

HRID 357726 반응식
[Br:1][CH2:2][CH:3]([C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([Cl:11])[CH:6]=1)[OH:4].CCCCCCCC(OC(CCCCCCC)=O)=O.C(OC=C)(=O)CCCCCCCCCCC.C(OC(C)C)(C)C>>[Br:1][CH2:2][C@@H:3]([C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([Cl:11])[CH:6]=1)[OH:4]

참가 물질

5

실험 절차

To a mixture of 100 mg (0.4 mmol) of 2-bromo-1-(3-chlorophenyl)ethanol, 10 mg of TOYOCHIMU LIP (available from Toyobo Co., Ltd.) and 100 mg (0.31 mmol) of n-caprylic anhydride or 61 mg (0.27 mmol) of vinyl laurate as an acylating agent was added isopropyl ether to make the total volume 1 ml. The reaction mixtures were respectively allowed to undergo reaction at a temperature of 27° C. for 30 hours. After the termination of the reaction, the reaction system was subjected to centrifugal filtration to remove the supernatant. To the reaction system was then added another batch of 2-bromo-1-(3-chlorophenyl)ethanol, the acylating agent and diisopropyl ether to make the total volume 1 ml. The same reaction was then repeated twice. The initial rate and total activity at the various steps are set forth in Table 5. The initial rate is represented relative to that at the 1st step as 100%. Activity=total amount of converted BH/enzyme weight.

후처리

  1. customThe reaction mixtures
  2. customreaction at a temperature of 27° C. for 30 hours
  3. customAfter the termination of the reaction
  4. filtrationthe reaction system was subjected to centrifugal filtration
  5. customto remove the supernatant
  6. additionTo the reaction system was then added another batch of 2-bromo-1-(3-chlorophenyl)ethanol
  7. customThe same reaction

출처 및 근거

ORD 기록
ord-2d8910f2b32d45dbbae9fea2b14ba90e
출처 데이터셋
uspto-grants-1998_11
특허 번호
US05841001

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