L-Homoserine → Cbz-L-Homoserine

HRID 1292643

반응식

HRID 1292643 반응식
[CH2:1]([O:8][C:9]([O:11]N1C(=O)CCC1=O)=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[NH2:19][C@H:20]([C:24]([OH:26])=[O:25])[CH2:21][CH2:22][OH:23].C(=O)(O)[O-].[Na+]>O.CC(C)=O>[C:2]1([CH2:1][O:8][C:9]([NH:19][C@H:20]([C:24]([OH:26])=[O:25])[CH2:21][CH2:22][OH:23])=[O:11])[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

참가 물질

6

실험 절차

N-(Benzyloxycarbonyloxy)succinimide (23.57 g., 94.58 mmol.) was added to a solution of L-homoserine (10.24 g., 85.98 mmol.) and sodium bicarbonate (7.95 g., 94.58 mmol., 1.1 eq.) in a mixture of water (100 ml.) and acetone (100 ml.). The mixture was stirred at room temperature overnight. The acetone was removed under reduced pressure (rotovap) and the aqueous solution was washed with methylene chloride (2×75 ml.). The aqueous layer was then acidified to pH 2 by addition of 6N hydrochloric acid and extracted with ethyl acetate (2×250 ml.). The combined ethyl acetate layers were washed with water (2×100 ml.) and brine, dried over sodium sulfate, filtered, concentrated and dried in vacuo to afford 19.54 g. of title product as a white solid. TLC (ethyl acetate:n-butanol:acetic acid:water; 2:1:1:1) Rf =0.74

후처리

  1. customThe acetone was removed under reduced pressure (rotovap)
  2. washthe aqueous solution was washed with methylene chloride (2×75 ml.)
  3. additionThe aqueous layer was then acidified to pH 2 by addition of 6N hydrochloric acid
  4. extractionextracted with ethyl acetate (2×250 ml.)
  5. washThe combined ethyl acetate layers were washed with water (2×100 ml.) and brine
  6. dry with materialdried over sodium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated
  9. customdried in vacuo
  10. customto afford 19.54 g

출처 및 근거

ORD 기록
ord-24c41a44e170435cb8687265e8fd2648
출처 데이터셋
uspto-grants-1998_05
특허 번호
US05756832

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