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Methylamine → ethyl (2S,3R)-3-t-butyldimethylsilyloxy-2-(methylaminomethyl)butanoate

HRID 1975477
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인쇄 미리보기

반응식

HRID 1975477 반응식
[Si:1]([O:8][C@H:9]([CH3:17])[C:10](=[CH2:16])[C:11]([O:13][CH2:14][CH3:15])=[O:12])([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2].[CH3:18][NH2:19]>CO>[Si:1]([O:8][C@H:9]([CH3:17])[C@H:10]([CH2:16][NH:19][CH3:18])[C:11]([O:13][CH2:14][CH3:15])=[O:12])([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:2])[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6329MethylamineHCID 11108029ethyl 2-[(1R)-1-(t-butyldimethylsilyloxy)ethyl]acrylate

생성물 1

HCID 57178030ethyl (2S,3R)-3-t-butyldimethylsilyloxy-2-(methylaminomethyl)butanoate

시약·촉매·용매 1

HCID 887Methanol용매2회

실험 절차

To a solution of ethyl (3R)-3-t-butyldimethylsilyloxy-2-methylidenebutanoate (130 g) in methanol (1.3 l) was added a solution of 30% methylamine in methanol (63 ml). The resulting mixture was allowed to stir at ambient temperature for 2 days. Evaporation of the solvent gave ethyl (2S,3R)-3-t-butyldimethylsilyloxy-2-(methylaminomethyl)butanoate (150.0 g).

후처리

  1. customEvaporation of the solvent

출처 및 근거

ORD 기록
ord-3ddd4a458c2b4f6b86be2eb0cce87887
출처 데이터셋
uspto-grants-1994_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05286721

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