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

Ethyl chloroformate → [2-(2-fluorobenzoyl)-1H-pyrrol-1-yl]carbamic acid, ethyl ester

HRID 280131
노트
인쇄 미리보기

반응식

HRID 280131 반응식
[NH2:1][N:2]1[CH:6]=[CH:5][CH:4]=[C:3]1[C:7](=[O:15])[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=1[F:14].C(=O)(O)[O-].[Na+].Cl[C:22]([O:24][CH2:25][CH3:26])=[O:23]>ClCCl>[F:14][C:9]1[CH:10]=[CH:11][CH:12]=[CH:13][C:8]=1[C:7]([C:3]1[N:2]([NH:1][C:22](=[O:23])[O:24][CH2:25][CH3:26])[CH:6]=[CH:5][CH:4]=1)=[O:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 10928Ethyl chloroformateHCID 516892Sodium BicarbonateHCID 134577161-Amino-2-(2-fluorobenzoyl)pyrrole

생성물 1

HCID 13457759[2-(2-fluorobenzoyl)-1H-pyrrol-1-yl]carbamic acid, ethyl ester수율 92%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

1-Amino-2-(2-fluorobenzoyl)pyrrole (41 g, 0.20 mol) and sodium bicarbonate (39 g, 0.46 mol) were combined in 400 ml of dichloromethane. To this stirred slurry was added ethyl chloroformate (24 g, 0.22 mol) over 3 minutes and the reaction mixture was refluxed for 5 hours, whereupon it was quenched with 200 ml of H2O and the organic layer separated. The organic extract was washed with H2O and brine, dried (MgSO4), filtered, and evaporated to an oil which crystallized upon trituration with hexane. Filtration yielded 50.8 g (92%) of crystals, m.p. 78°-80°.

후처리

  1. temperaturethe reaction mixture was refluxed for 5 hours, whereupon it
  2. customwas quenched with 200 ml of H2O
  3. customthe organic layer separated
  4. extractionThe organic extract
  5. washwas washed with H2O and brine
  6. dry with materialdried (MgSO4)
  7. filtrationfiltered
  8. customevaporated to an oil which
  9. customcrystallized upon trituration with hexane
  10. filtrationFiltration

출처 및 근거

ORD 기록
ord-440dd49913d7410eb93bed8edd54f69a
출처 데이터셋
uspto-grants-1986_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04588727

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트