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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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2-Propenoic acid, 2-cyano-3-ethoxy-, ethyl ester → HCID 67795583, 화합물

HRID 2082400
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HRID 2082400 반응식
[F:1][C:2]([F:15])([F:14])[C:3]1[CH:8]=[CH:7][C:6]([NH:9][NH2:10])=[C:5]([N+:11]([O-:13])=[O:12])[CH:4]=1.[C:16]([C:18](=[CH:24]OCC)[C:19]([O:21][CH2:22][CH3:23])=[O:20])#[N:17]>C(O)C>[C:16]([C:18](=[CH:24][NH:10][NH:9][C:6]1[CH:7]=[CH:8][C:3]([C:2]([F:14])([F:15])[F:1])=[CH:4][C:5]=1[N+:11]([O-:13])=[O:12])[C:19]([O:21][CH2:22][CH3:23])=[O:20])#[N:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 789432-Propenoic acid, 2-cyano-3-ethoxy-, ethyl esterHCID 38380972-nitro-4-(trifluoromethyl)phenylhydrazine

생성물 1

HCID 67795583HCID 67795583, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

4-Trifluoromethyl-2-nitrophenylhydrazine (13.5 g) and ethyl 2-cyano-3-ethoxyacrylate (10.3 g) were heated under reflux in ethanol (300 ml) for 24 hours. The solvent was removed under reduced pressure and the resulting residue triturated with dichloromethane/hexane to give ethyl 2-cyano-3-(2-nitro-4-trifluoromethylphenylhydrazino)acrylate, m.p. 163°-164°.

후처리

  1. customThe solvent was removed under reduced pressure
  2. customthe resulting residue triturated with dichloromethane/hexane

출처 및 근거

ORD 기록
ord-4183c844289c4cfa9bb7740055dfbf47
출처 데이터셋
uspto-grants-1993_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05189053

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