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

Diphosgene → 1-(4-Isocyanatophenyl)piperidin-2-one

HRID 496039
노트
인쇄 미리보기

반응식

HRID 496039 반응식
Cl[C:2](OC(Cl)(Cl)Cl)=[O:3].[NH2:9][C:10]1[CH:15]=[CH:14][C:13]([N:16]2[CH2:21][CH2:20][CH2:19][CH2:18][C:17]2=[O:22])=[CH:12][CH:11]=1>C1COCC1>[N:9]([C:10]1[CH:15]=[CH:14][C:13]([N:16]2[CH2:21][CH2:20][CH2:19][CH2:18][C:17]2=[O:22])=[CH:12][CH:11]=1)=[C:2]=[O:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 10426DiphosgeneHCID 114581781-(4-Aminophenyl)piperidin-2-one

생성물 1

HCID 111952821-(4-Isocyanatophenyl)piperidin-2-one

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

1.2 0.032 ml of trichloromethyl chloroformate is added under a nitrogen atmosphere to a solution of 50 mg of 1-(4-aminophenyl)piperidin-2-one (prepared from 1-(4-nitrophenyl)piperidin-2-one by hydrogenation using Raney nickel as catalyst) in 5 ml of THF, and the mixture is subsequently refluxed for 1.5 hours, giving 1-(4-isocyanatophenyl)piperidin-2-one (“AB”).

후처리

  1. temperaturethe mixture is subsequently refluxed for 1.5 hours

출처 및 근거

ORD 기록
ord-8cdb87b54c0b4dbcac7f853bfa815304
출처 데이터셋
uspto-grants-2005_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06943179B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트