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

Thionyl Chloride → 2-Propenoyl chloride, 3-(3-nitrophenyl)-, (E)-

HRID 848501
노트
인쇄 미리보기

반응식

HRID 848501 반응식
[N+:1]([C:4]1[CH:5]=[C:6]([CH:10]=[CH:11][C:12]([OH:14])=O)[CH:7]=[CH:8][CH:9]=1)([O-:3])=[O:2].S(Cl)([Cl:17])=O>C1C=CC=CC=1>[N+:1]([C:4]1[CH:5]=[C:6]([CH:10]=[CH:11][C:12]([Cl:17])=[O:14])[CH:7]=[CH:8][CH:9]=1)([O-:3])=[O:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24386Thionyl ChlorideHCID 683902-Propenoic acid, 3-(3-nitrophenyl)-

생성물 1

HCID 534112912-Propenoyl chloride, 3-(3-nitrophenyl)-, (E)-수율 91%

시약·촉매·용매 1

HCID 241Benzene용매

실험 절차

A mixture of 50 g. of 3-(3-nitrophenyl)propenoic acid, 24.54 ml. of thionyl chloride and 300 ml. of benzene were heated under reflux for 2.5 hours. The cooled solution was filtered and then it was evaporated in vacuo. The residue was recrystallized from carbon tetrachloride, to give 49.9 g. (91% yield) of the title compound, m.p. 81°-83.5° C.

후처리

  1. additionA mixture of 50 g
  2. temperatureunder reflux for 2.5 hours
  3. filtrationThe cooled solution was filtered
  4. customit was evaporated in vacuo
  5. customThe residue was recrystallized from carbon tetrachloride
  6. customto give 49.9 g

출처 및 근거

ORD 기록
ord-4bc709618a3446d399e48fd5ecd351b6
출처 데이터셋
uspto-grants-1981_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04296120

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트