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

Benzoyl chloride → 4-(3-Benzoyl-4-methoxyphenyl)-2-butanone

HRID 1074571
노트
인쇄 미리보기

반응식

HRID 1074571 반응식
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([CH2:9][CH2:10][C:11](=[O:13])[CH3:12])=[CH:5][CH:4]=1.[C:14](Cl)(=[O:21])[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1.[Cl-].[Al+3].[Cl-].[Cl-]>C(Cl)Cl>[C:14]([C:4]1[CH:5]=[C:6]([CH2:9][CH2:10][C:11](=[O:13])[CH3:12])[CH:7]=[CH:8][C:3]=1[O:2][CH3:1])(=[O:21])[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7412Benzoyl chlorideHCID 61007AnisylacetoneHCID 6451240Aluminum(III) Chloride

생성물 1

HCID 204960374-(3-Benzoyl-4-methoxyphenyl)-2-butanone수율 49.2%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a stirred mixture of 4-(4-methoxyphenyl)-2-butanone (15.4 g.), benzoyl chloride (13 g.) and methylene chloride (250 ml) at 0° C. was added portionwise aluminium chloride (23 g.) over a 20 minute period. The mixture was stirred a further 1 hour at room temperature and then poured onto ice and worked up in the usual way. Distillation of the product gave 4-(3-benzoyl-4-methoxyphenyl)-2-butanone (12 g.), b.p. 188°-192° C. (0.01 mm).

후처리

  1. additionpoured onto ice
  2. distillationDistillation of the product

출처 및 근거

ORD 기록
ord-e336def680134552895240deed2741ac
출처 데이터셋
uspto-grants-1983_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04393079

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트