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Phenyl chloroformate → 4-Phenoxycarbonyl-2-toluene-p-sulphonyloxymethylmorpholine

HRID 1283100
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반응식

HRID 1283100 반응식
C([N:8]1[CH2:13][CH2:12][O:11][CH:10]([CH2:14][O:15][S:16]([C:19]2[CH:24]=[CH:23][C:22]([CH3:25])=[CH:21][CH:20]=2)(=[O:18])=[O:17])[CH2:9]1)C1C=CC=CC=1.[C:26]1([O:32][C:33](Cl)=[O:34])[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1>ClCCl>[O:32]([C:33]([N:8]1[CH2:13][CH2:12][O:11][CH:10]([CH2:14][O:15][S:16]([C:19]2[CH:24]=[CH:23][C:22]([CH3:25])=[CH:21][CH:20]=2)(=[O:17])=[O:18])[CH2:9]1)=[O:34])[C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 15891Phenyl chloroformateHCID 122977674-Benzyl-2-toluene-p-sulphonyloxymethylmorpholine

생성물 1

HCID 214303984-Phenoxycarbonyl-2-toluene-p-sulphonyloxymethylmorpholine

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution of 4-benzyl-2-toluene-p-sulphonyloxymethylmorpholine (5 g.) in dichloromethane (50 ml.), phenylchloroformate (2 ml.) is added and the mixture is stirred at ambient temperature (ca 20°C) for 24 hours. The solvent is evaporated and the residual oil is recrystallised from ethanol to give 4-phenoxycarbonyl-2-toluene-p-sulphonyloxymethylmorpholine, m.p. 101°-103°C.

후처리

  1. customThe solvent is evaporated
  2. customthe residual oil is recrystallised from ethanol

출처 및 근거

ORD 기록
ord-13950243af1743bea91d5d47a92c6bc1
출처 데이터셋
uspto-grants-1976_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03974158

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