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

Ethyl 3-(2-chloro-4,5-difluorophenyl)-3-oxopropanoate → Ethyl 2-(2-chloro-4,5-difluorobenzoyl)-3-ethoxyacrylate

HRID 982207
노트
인쇄 미리보기

반응식

HRID 982207 반응식
[Cl:1][C:2]1[CH:15]=[C:14]([F:16])[C:13]([F:17])=[CH:12][C:3]=1[C:4]([CH2:6][C:7]([O:9][CH2:10][CH3:11])=[O:8])=[O:5].[CH:18]([O-])([O-])[O:19][CH2:20][CH3:21]>C(OC(=O)C)(=O)C>[Cl:1][C:2]1[CH:15]=[C:14]([F:16])[C:13]([F:17])=[CH:12][C:3]=1[C:4]([C:6](=[CH:18][O:19][CH2:20][CH3:21])[C:7]([O:9][CH2:10][CH3:11])=[O:8])=[O:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14423850Ethyl 3-(2-chloro-4,5-difluorophenyl)-3-oxopropanoateHCID 53630039Ethylorthoformate

생성물 1

HCID 54163438Ethyl 2-(2-chloro-4,5-difluorobenzoyl)-3-ethoxyacrylate수율 98.7%

시약·촉매·용매 1

HCID 7918Acetic Anhydride용매

실험 절차

Into a 200 cc glass reactor equipped with a stirrer, 26.3 g of ethyl 2-chloro-4,5-difluorobenzoylacetate, 23.7 g of ethyl ortho-formate and 40 ml of acetic anhydride were charged, and reacted at a reaction temperature of from 120° to 135° C. After completion of the reaction, the reaction mixture was concentrated by distillation under reduced pressure to obtain 31.5 g of the desired compound as the residue.

후처리

  1. customInto a 200 cc glass reactor equipped with a stirrer
  2. customreacted at a reaction temperature of from 120° to 135° C
  3. customAfter completion of the reaction
  4. concentrationthe reaction mixture was concentrated by distillation under reduced pressure

출처 및 근거

ORD 기록
ord-d01b41c6023a42428ba2b3990f589848
출처 데이터셋
uspto-grants-1991_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04994610

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트