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Trifluoroacetic acid → (E)-2-(4-chloro-6-fluoro-1-indanylidene)acetic acid

HRID 726149
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반응식

HRID 726149 반응식
FC(F)(F)C(O)=O.[Cl:8][C:9]1[CH:17]=[C:16]([F:18])[CH:15]=[C:14]2[C:10]=1[CH2:11][CH2:12][C:13]2([CH2:20][C:21]([OH:23])=[O:22])O>ClCCl>[Cl:8][C:9]1[CH:17]=[C:16]([F:18])[CH:15]=[C:14]2[C:10]=1[CH2:11][CH2:12]/[C:13]/2=[CH:20]\[C:21]([OH:23])=[O:22]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 110860282-(4-Chloro-6-fluoro-1-hydroxy-1-indanyl)acetic acid

생성물 1

HCID 11031575(E)-2-(4-chloro-6-fluoro-1-indanylidene)acetic acid수율 93.5%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

Trifluoroacetic acid (27.4 ml) was added to a stirred, chilled (ice-methanol bath) solution of 2-(4-chloro-6-fluoro-1-hydroxy-1-indanyl)acetic acid (12.5 g, 0.05 mol) in dichloromethane (200 ml). After 1.5 h, the mixture was concentrated in vacuo. Dichloromethane was added to the residue and the mixture was concentrated in vacuo to give 10.6 g of crude (E)-2-(4-chloro-6-fluoro-1-indanylidene)acetic acid. Chromatography of a 1.0 g sample on silica gel with ethyl acetate:hexanes (1:1) as eluent gave 0.32 g of (E)-2-(4-chloro-6-fluoro-1-indanylidene)acetic acid as a white solid: mp 229°-230° C.

후처리

  1. concentrationthe mixture was concentrated in vacuo
  2. additionDichloromethane was added to the residue
  3. concentrationthe mixture was concentrated in vacuo

출처 및 근거

ORD 기록
ord-db283d9ef86f4447b37f32f7eedb41f3
출처 데이터셋
uspto-grants-1998_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05708033

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