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Benzoyl isothiocyanate → t-Butyl 3-amino-2-(N-benzoylthiocarbamoyl)crotonate

HRID 434335
노트
인쇄 미리보기

반응식

HRID 434335 반응식
[NH2:1]/[C:2](/[CH3:11])=[CH:3]\[C:4]([O:6][C:7]([CH3:10])([CH3:9])[CH3:8])=[O:5].[C:12]([N:20]=[C:21]=[S:22])(=[O:19])[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1>C(OCC)C>[NH2:1]/[C:2](/[CH3:11])=[C:3](/[C:21](=[S:22])[NH:20][C:12](=[O:19])[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)\[C:4]([O:6][C:7]([CH3:10])([CH3:9])[CH3:8])=[O:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 68284Benzoyl isothiocyanateHCID 12221517tert-Butyl 3-aminocrotonate

생성물 1

HCID 86738557t-Butyl 3-amino-2-(N-benzoylthiocarbamoyl)crotonate수율 43.7%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

A mixture of t-butyl 3-aminocrotonate (65.3 g, 0.4 mol), benzoyl isothiocyanate (62.9 g, 0.4 mol), and diethyl ether (300 ml) was stirred at ambient temperature for 3 hours. The solid product was collected on a filter, washed with ether and dried to give 56 g (43.7 percent yield) of material melting at 107° to 110° C.

후처리

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  1. customThe solid product was collected on a filter
  2. washwashed with ether
  3. customdried

출처 및 근거

ORD 기록
ord-bd49efada2154587980ccd638fa57869
출처 데이터셋
uspto-grants-1983_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04396546

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