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Anisole → 2-(4-chlorophenyl)-1-(4-methoxyphenyl)ethanone

HRID 1813935
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인쇄 미리보기

반응식

HRID 1813935 반응식
[C:1]1([O:7][CH3:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Cl:9][C:10]1[CH:15]=[CH:14][C:13]([CH2:16][C:17](O)=[O:18])=[CH:12][CH:11]=1.FC(F)(F)C(OC(=O)C(F)(F)F)=O>>[Cl:9][C:10]1[CH:15]=[CH:14][C:13]([CH2:16][C:17]([C:4]2[CH:5]=[CH:6][C:1]([O:7][CH3:8])=[CH:2][CH:3]=2)=[O:18])=[CH:12][CH:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 7519AnisoleHCID 9845Trifluoroacetic anhydrideHCID 15880(4-Chlorophenyl)acetic acid

생성물 1

HCID 4572422-(4-chlorophenyl)-1-(4-methoxyphenyl)ethanone

실험 절차

Anisole (13.9 g, 0.13 mol) is added to a stirred solution of 4-chlorophenylacetic acid (20.0 g, 0.12 mol) in trifluoroacetic anhydride (16.5 ml, 0.12 mol). The mixture is stirred in room temperature for 24 h. Ice water is added and the crystallized product is collected on a sinter and washed with water. The product is recrystallized from ethanol. The yield is 20.4 g, 67%.

후처리

  1. customthe crystallized product is collected on a sinter
  2. washwashed with water
  3. customThe product is recrystallized from ethanol

출처 및 근거

ORD 기록
ord-685ae380c7204a3cb61eecb7df8b0662
출처 데이터셋
uspto-grants-2005_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06875775B2

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