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

Thionyl Chloride → 4-Bromo-3-methylthiophene-2-carbonyl chloride

HRID 2269671
노트
인쇄 미리보기

반응식

HRID 2269671 반응식
[Br:1][C:2]1[C:3]([CH3:10])=[C:4]([C:7](O)=[O:8])[S:5][CH:6]=1.S(Cl)([Cl:13])=O>CN(C=O)C.ClCCCl>[Br:1][C:2]1[C:3]([CH3:10])=[C:4]([C:7]([Cl:13])=[O:8])[S:5][CH:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 24386Thionyl ChlorideHCID 27570734-Bromo-3-methylthiophenecarboxylic acid

생성물 1

HCID 27570744-Bromo-3-methylthiophene-2-carbonyl chloride수율 100.2%

시약·촉매·용매 2

HCID 6228Dimethylformamide촉매HCID 111,2-Dichloroethane용매

실험 절차

A slurry of 1.11 g (5 mmole) of 4-bromo-3-methyl-2-thiophenecarboxylic acid, 0.44 mL (6 mmole) of thionyl chloride, 5 drops of DMF, and 10 mL of 1,2-dichloroethane was heated at 80° C. for 1.5 h. The clear solution was cooled and concentrated on a roto-evaporator. The residue was dissolved in 5 mL of 1,2-dichloroethane and reconcentrated on a roto-evaporator to give 1.2 g of a tan solid, 97% pure (GC area). This acid chloride was used without further purification.

후처리

  1. temperatureThe clear solution was cooled
  2. concentrationconcentrated on a roto-evaporator
  3. dissolutionThe residue was dissolved in 5 mL of 1,2-dichloroethane
  4. customreconcentrated on a roto-evaporator

출처 및 근거

ORD 기록
ord-dd58aa7ca3fa4d66aeee2cca4d152b3d
출처 데이터셋
uspto-grants-2001_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06329528B1

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트