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Phosgene → Thiomorpholine-4-carbonyl chloride

HRID 1291761
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HRID 1291761 반응식
[NH:1]1[CH2:6][CH2:5][S:4][CH2:3][CH2:2]1.[C:7](Cl)([Cl:9])=[O:8]>C1(C)C=CC=CC=1>[N:1]1([C:7]([Cl:9])=[O:8])[CH2:6][CH2:5][S:4][CH2:3][CH2:2]1
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참가 물질

4

반응물 2

HCID 6371Phosgene2회HCID 67164Thiomorpholine

생성물 1

HCID 19080217Thiomorpholine-4-carbonyl chloride

시약·촉매·용매 1

HCID 1140Toluene용매2회

실험 절차

A solution of 10 g (97 mmol) of thiomorpholine in 200 ml of toluene is added dropwise at 0° to a solution of 85 ml (165 mmol) of 20% phosgene in toluene and the white suspension is stirred for 1 h at RT. Excess phosgene is driven off by introducing nitrogen, the suspension is filtered, and the filtrate is concentrated by evaporation. The title compound is obtained in the form of a yellow oil. IR (CH2Cl2, cm-1): 1735, 1450, 1440, 1405, 1370, 1290, 1180.

후처리

  1. additionby introducing nitrogen
  2. filtrationthe suspension is filtered
  3. concentrationthe filtrate is concentrated by evaporation

출처 및 근거

ORD 기록
ord-c580a4603e7c4806b30536f8fab50c42
출처 데이터셋
uspto-grants-1998_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05753652

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