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Diazomethane → HCID 54488354, 화합물

HRID 1395131
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HRID 1395131 반응식
[Cl:1][C:2]1[CH:18]=[CH:17][C:5]([CH2:6][NH:7][C:8]([S:10][CH2:11][CH2:12][CH2:13][C:14]([OH:16])=[O:15])=[S:9])=[CH:4][CH:3]=1.[N+](=[CH2:21])=[N-]>C(OCC)C>[CH3:21][O:15][C:14](=[O:16])[CH2:13][CH2:12][CH2:11][S:10][C:8](=[S:9])[NH:7][CH2:6][C:5]1[CH:17]=[CH:18][C:2]([Cl:1])=[CH:3][CH:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 9550DiazomethaneHCID 203402724-{[(p-Chlorobenzyl)thiocarbamoyl]thio}-butyric acid

생성물 1

HCID 54488354HCID 54488354, 화합물

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

1.5 G. of 4-{[(p-chlorobenzyl)thiocarbamoyl]thio}-butyric acid were dissolved in 30 ml. of diethyl ether and treated with an excess of an ethereal diazomethane solution. The resulting solution was evaporated. The residue was recrystallized from cyclohexane, and 1.2 g. of 4-{[(p-chlorobenzyl)thiocarbamoyl]thio}-butyric acid methyl ester having a melting point of 60°-62° C. were obtained.

후처리

  1. customThe resulting solution was evaporated
  2. customThe residue was recrystallized from cyclohexane, and 1.2 g

출처 및 근거

ORD 기록
ord-eff9508acb444f87b1c47e2088508cdd
출처 데이터셋
uspto-grants-1980_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04202832

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