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Lithium Hydroxide → (2R)-N-methanesulfonyl-(4-chlorophenyl)alanine

HRID 1670017
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인쇄 미리보기

반응식

HRID 1670017 반응식
C[O:2][C:3](=[O:18])[C@@H:4]([CH3:17])[N:5]([C:10]1[CH:15]=[CH:14][C:13]([Cl:16])=[CH:12][CH:11]=1)[S:6]([CH3:9])(=[O:8])=[O:7].[Li+].[OH-]>O.CO>[CH3:9][S:6]([N:5]([C:10]1[CH:11]=[CH:12][C:13]([Cl:16])=[CH:14][CH:15]=1)[C@@H:4]([C:3]([OH:18])=[O:2])[CH3:17])(=[O:7])=[O:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 3939Lithium HydroxideHCID 967649(2R)-N-methanesulfonyl-(4-chlorophenyl)alanine methyl ester

생성물 1

HCID 967528(2R)-N-methanesulfonyl-(4-chlorophenyl)alanine수율 94.3%

시약·촉매·용매 1

HCID 22242641Methanol--water (1/1)용매

실험 절차

To a solution of (2R)-N-methanesulfonyl-(4-chlorophenyl)alanine methylester, prepared in Step A, in water/methanol (5 mL, 1/1) was added portionwise LiOH (70.0 mg, 2.00 mmol). After being stirred at rt for 3 h, the reaction mixture was concentrated, and the residue was diluted with 1N HCl solution. The organic material was extracted with EtOAc, the extracts were concentrated in vacuo to give the title compound (179 mg, 94.3%).

후처리

  1. concentrationthe reaction mixture was concentrated
  2. additionthe residue was diluted with 1N HCl solution
  3. extractionThe organic material was extracted with EtOAc
  4. concentrationthe extracts were concentrated in vacuo

출처 및 근거

ORD 기록
ord-17e24dfe560444e78f5a74562a9c6df4
출처 데이터셋
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07989634B2

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