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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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p-Bromocinnamic acid → 3-(4-Bromophenyl)prop-2-enoyl chloride

HRID 2289798
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HRID 2289798 반응식
BrC1C=C2C(C(Cl)=CN=C2[Cl:12])=CC=1.[Br:14][C:15]1[CH:25]=[CH:24][C:18]([CH:19]=[CH:20][C:21](O)=[O:22])=[CH:17][CH:16]=1>O=S(Cl)Cl>[Br:14][C:15]1[CH:25]=[CH:24][C:18]([CH:19]=[CH:20][C:21]([Cl:12])=[O:22])=[CH:17][CH:16]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 99777p-Bromocinnamic acidHCID 166583507-Bromo-1,4-dichloroisoquinoline

생성물 1

HCID 534112933-(4-Bromophenyl)prop-2-enoyl chloride

시약·촉매·용매 1

HCID 24386Thionyl Chloride용매

실험 절차

7-Bromo-1,4-dichloroisoquinoline ##STR100## A solution of 4-bromocinnamic acid (5.03 g, 22.2 mmol) in SOCl2 (15 mL) was stirred at 23° C. for 16 h, and then heated at reflux for a further 2 h. The solvents were evaporated in vacuo and the residue azeotroped with PhMe (×3) to yield 4-bromocinnamoyl chloride (22 mmol) as an orange-brown solid.

후처리

  1. temperatureheated
  2. temperatureat reflux for a further 2 h
  3. customThe solvents were evaporated in vacuo
  4. customthe residue azeotroped with PhMe (×3)

출처 및 근거

ORD 기록
ord-8fd47bf109574ab49119dd7afc3a2cdc
출처 데이터셋
uspto-grants-2000_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06093731

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