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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Thionyl Chloride → p-Cyanocinnamic acid chloride

HRID 1439141
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HRID 1439141 반응식
S(Cl)([Cl:3])=O.[C:5]([C:7]1[CH:17]=[CH:16][C:10]([CH:11]=[CH:12][C:13](O)=[O:14])=[CH:9][CH:8]=1)#[N:6]>>[C:5]([C:7]1[CH:17]=[CH:16][C:10]([CH:11]=[CH:12][C:13]([Cl:3])=[O:14])=[CH:9][CH:8]=1)#[N:6]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 24386Thionyl ChlorideHCID 86773p-Cyanocinnamic acid

생성물 1

HCID 54112663p-Cyanocinnamic acid chloride

반응 조건

온도
80 °C

실험 절차

0.2mol of p-cyanobenzaldehyde and 0.3mol of malonic acid were dissolved in 80ml of pyridine at room temperature, and 30 drops of piperidine were added thereto. The mixture was heated and stirred for 4 hours at about 100° C. After the reaction, the solution was poured slowly into dilute hydrochloric acid (250ml hydrochloric acid/250g water). Then, the resulting white precipitate was separated by filtering and washed with dilute hydrochloric acid and water, and was recrystallized by use of glacial acetic acid to obtain p-cyanocinnamic acid. 0.3mol of thionyl chloride was added to 0.1mol of the p-cyanocinnamic acid and the mixture was heated and stirred at about 80° C for 3 hours. An excess thionyl chloride was then removed under reduced pressure to obtain p-cyanocinnamic acid chloride.

후처리

  1. temperaturethe mixture was heated
  2. customAn excess thionyl chloride was then removed under reduced pressure

출처 및 근거

ORD 기록
ord-6fb080a787654cc29bbdfe03dedec883
출처 데이터셋
uspto-grants-1977_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04058475

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