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

Thionyl Chloride → Methyl 3-chlorocarbonyl-2,4-dichlorobenzoate

HRID 377546
노트
인쇄 미리보기

반응식

HRID 377546 반응식
S(Cl)([Cl:3])=O.[Cl:5][C:6]1[C:15]([C:16](O)=[O:17])=[C:14]([Cl:19])[CH:13]=[CH:12][C:7]=1[C:8]([O:10][CH3:11])=[O:9]>CN(C)C=O.C1(C)C=CC=CC=1>[Cl:3][C:16]([C:15]1[C:6]([Cl:5])=[C:7]([CH:12]=[CH:13][C:14]=1[Cl:19])[C:8]([O:10][CH3:11])=[O:9])=[O:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 24386Thionyl ChlorideHCID 18517411Methyl 2,4-dichloro-3-hydroxycarbonylbenzoate

생성물 1

HCID 18517406Methyl 3-chlorocarbonyl-2,4-dichlorobenzoate수율 100%

시약·촉매·용매 2

HCID 6228Dimethylformamide촉매HCID 1140Toluene용매

실험 절차

Two drops of dimethylformamide and 11.90 g (0.1 mol) of thionyl chloride were added to a solution of 5.00 g (0.02 mol) of methyl 2,4-dichloro-3-hydroxycarbonylbenzoate and 50 ml of dry toluene. The solution was refluxed for 4 hours. After the solvent had been distilled off, 5.35 g of methyl 3-chlorocarbonyl-2,4-dichlorobenzoate were obtained.

후처리

  1. temperatureThe solution was refluxed for 4 hours
  2. distillationAfter the solvent had been distilled off

출처 및 근거

ORD 기록
ord-93f4750ce6a54134adb0ffd9dc0de74a
출처 데이터셋
uspto-grants-2000_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06028035

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트