홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Imidazole → alpha-Chloroethoxycarbonylimidazole

HRID 4431
노트
인쇄 미리보기

반응식

HRID 4431 반응식
Cl[C:2]([O:4][CH2:5][CH2:6]Cl)=[O:3].[NH:8]1[CH:12]=[CH:11][N:10]=[CH:9]1.O.[Cl:14]CCl>>[Cl:14][CH:5]([O:4][C:2]([C:9]1[NH:8][CH:12]=[CH:11][N:10]=1)=[O:3])[CH3:6]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 795ImidazoleHCID 962WaterHCID 6344DichloromethaneHCID 123052-Chloroethyl chloroformate

생성물 1

HCID 20152581alpha-Chloroethoxycarbonylimidazole

실험 절차

28.6 g (0.2 mole) of chloroethyl chloroformate are added dropwise to a solution of 27.2 g (0.4 mole) of imidazole in 200 ml of dichloromethane cooled in a water bath. The mixture is stirred at room temperature for 4 hours, and 50 ml of iced water are then added. The organic phase is washed with 2×50 ml of water and then dried over magnesium sulphate. After evaporation and distillation, 38.1 g (73%) of α-chloroethoxycarbonylimidazole [B.p. 80° C./66.6 Pa (0.5 mm Hg)] are obtained in the form of a colourless liquid which crystallises spontaneously at room temperature, m.p. 50° C. ##STR57##

후처리

  1. temperaturecooled in a water bath
  2. washThe organic phase is washed with 2×50 ml of water
  3. dry with materialdried over magnesium sulphate
  4. customAfter evaporation and distillation, 38.1 g (73%) of α-chloroethoxycarbonylimidazole [B.p. 80° C./66.6 Pa (0.5 mm Hg)]
  5. customare obtained in the form of a colourless liquid which
  6. customcrystallises spontaneously at room temperature

출처 및 근거

ORD 기록
ord-a75633828b0a48b69e9a6ab1c8a89eba
출처 데이터셋
uspto-grants-1988_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04725680

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트