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

Oxalyl chloride → HCID 20096059, 화합물

HRID 1708933
노트
인쇄 미리보기

반응식

HRID 1708933 반응식
C(Cl)(=O)[C:2](Cl)=[O:3].[Cl:7][C:8]1[C:16]([N+:17]([O-:19])=[O:18])=[CH:15][CH:14]=[C:13]([Cl:20])[C:9]=1[C:10]([NH2:12])=[O:11]>C(Cl)Cl>[Cl:7][C:8]1[C:16]([N+:17]([O-:19])=[O:18])=[CH:15][CH:14]=[C:13]([Cl:20])[C:9]=1[C:10]([N:12]=[C:2]=[O:3])=[O:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 65578Oxalyl chlorideHCID 133824032,6-Dichloro-3-nitrobenzamide

생성물 1

HCID 20096059HCID 20096059, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

3.5 ml of oxalyl chloride are added dropwise at room temperature over a period of 30 minutes to a suspension of 7.68 g of 2,6-dichloro-3-nitrobenzoic acid amide in 570 ml of methylene chloride. The batch is then heated at reflux temperature for 18 hours and the solvent is subsequently distilled off in vacuo, affording 8.6 g of crude 2,6-dichloro-3-nitrobenzoyl isocyanate which can be used directly in the subsequent reactions.

후처리

  1. temperatureThe batch is then heated
  2. temperatureat reflux temperature for 18 hours
  3. distillationthe solvent is subsequently distilled off in vacuo

출처 및 근거

ORD 기록
ord-1bc03376051142e9a3bf6638c75149f0
출처 데이터셋
uspto-grants-1990_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04946854

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트