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

Ethylenethiourea → 1-[1-(3,4-Dichlorophenyl)cyclobutyl]-2-(2-imidazolin-2-ylthio)ethanone hydrobromide

HRID 635338
노트
인쇄 미리보기

반응식

HRID 635338 반응식
[NH:1]1[CH2:5][CH2:4][NH:3][C:2]1=[S:6].[Br:7][CH2:8][C:9]([C:11]1([C:15]2[CH:20]=[CH:19][C:18]([Cl:21])=[C:17]([Cl:22])[CH:16]=2)[CH2:14][CH2:13][CH2:12]1)=[O:10]>CC(C)=O>[BrH:7].[Cl:22][C:17]1[CH:16]=[C:15]([C:11]2([C:9](=[O:10])[CH2:8][S:6][C:2]3[NH:1][CH2:5][CH2:4][N:3]=3)[CH2:14][CH2:13][CH2:12]2)[CH:20]=[CH:19][C:18]=1[Cl:21]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 2723650EthylenethioureaHCID 212584722-Bromo-1-[1-(3,4-dichlorophenyl)cyclobutyl]ethan-1-one

생성물 1

HCID 212585071-[1-(3,4-Dichlorophenyl)cyclobutyl]-2-(2-imidazolin-2-ylthio)ethanone hydrobromide수율 87.2%

시약·촉매·용매 1

HCID 180Acetone용매2회

실험 절차

A solution of imidazolidine-2-thione (4.5 g) in acetone (750 ml ) was added to a solution of 2-bromo-1-[1-(3,4-dichlorophenyl)cyclobutyl]ethanone (15 g) in acetone (125 ml), then the stirred mixture was heated under reflux for 10 minutes, and allowed to cool to ambient temperature. The resulting solid was collected by filtration, washed with ethanol (50 ml) and dried in vacuo at 60° C. for 4 hours to give 1-[1-(3,4-dichlorophenyl)cyclobutyl]-2-(2-imidazolin-2-ylthio)ethanone hydrobromide as a white solid (16.3 g), m.p. 156-158° C.

후처리

  1. temperaturethe stirred mixture was heated
  2. temperatureunder reflux for 10 minutes
  3. filtrationThe resulting solid was collected by filtration
  4. washwashed with ethanol (50 ml)
  5. customdried in vacuo at 60° C. for 4 hours

출처 및 근거

ORD 기록
ord-74e0418616e94647b676dce864778aaf
출처 데이터셋
uspto-grants-2001_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06187802B1

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트