Methyl 2-benzylprop-2-enoate → Methyl alpha-[[hydroxy[1-[[(phenylmethoxy)carbonyl]amino]ethyl]phosphinyl]methyl]benzenepropanoate

HRID 1058770노트

반응식

HRID 1058770 반응식
[PH2:1](=[O:3])[OH:2].[C:4]1([CH2:10][C:11](=[CH2:16])[C:12]([O:14][CH3:15])=[O:13])[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[CH3:17]/[C:18](/O[Si](C)(C)C)=[N:19]\[Si](C)(C)C.[C:29]([O:32][CH2:33][CH3:34])(=[O:31])C.O>C(#N)C>[OH:3][P:1]([CH2:16][CH:11]([CH2:10][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1)[C:12]([O:14][CH3:15])=[O:13])([CH:18]([NH:19][C:29]([O:32][CH2:33][C:34]1[CH:8]=[CH:9][CH:4]=[CH:5][CH:6]=1)=[O:31])[CH3:17])=[O:2]

참가 물질

6

실험 절차

A solution of 0.6 g (2.47 mmol) of 1-[[(phenylmethoxy)carbonyl]amino]ethyl]phosphinic acid, 2.17 g (12.3 mmol) of methyl 2-(phenylmethyl)propenoate and 0.52 ml of N,O-bis(trimethylsilyl)acetamide in 0.27 ml of acetonitrile is stirred at a temperature in the region of 20° C. for 24 hours. 60 ml of a 1/1 ethyl acetate/water mixture are added. The aqueous phase is extracted with ethyl acetate. The combined organic phases are washed with water, dried over sodium sulphate, filtered and evaporated off under vacuum. The product is purified by recrystallization from a mixture of ethyl acetate and hexane. 0.71 g of product are recovered (yield=68.9%).

후처리

  1. extractionThe aqueous phase is extracted with ethyl acetate
  2. washThe combined organic phases are washed with water
  3. dry with materialdried over sodium sulphate
  4. filtrationfiltered
  5. customevaporated off under vacuum
  6. customThe product is purified by recrystallization from a mixture of ethyl acetate and hexane
  7. custom0.71 g of product are recovered (yield=68.9%)

출처 및 근거

ORD 기록
ord-edf37c17871546aebbe58bab8a274b28
출처 데이터셋
uspto-grants-2003_02
특허 번호
US06518260B1

반응 노트

불러오는 중…