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1,3-Dibromopropane → 1-(3-Bromopropoxy)-4-(trifluoromethoxy)benzene

HRID 363085
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인쇄 미리보기

반응식

HRID 363085 반응식
[Br:1][CH2:2][CH2:3][CH2:4]Br.C(=O)([O-])[O-].[K+].[K+].[F:12][C:13]([F:23])([F:22])[O:14][C:15]1[CH:20]=[CH:19][C:18]([OH:21])=[CH:17][CH:16]=1>CN(C)C=O>[Br:1][CH2:2][CH2:3][CH2:4][O:21][C:18]1[CH:19]=[CH:20][C:15]([O:14][C:13]([F:12])([F:22])[F:23])=[CH:16][CH:17]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 80011,3-DibromopropaneHCID 11430Potassium CarbonateHCID 70015p-(Trifluoromethoxy)phenol

생성물 1

HCID 136722751-(3-Bromopropoxy)-4-(trifluoromethoxy)benzene수율 60.2%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매2회

실험 절차

To a mixture of 20.4 g of 1,3-dibromopropane, 7.1 g of potassium carbonate and 100 ml of N,N-dimethylformamide was added dropwise a solution of 9 g of 4-trifluoromethoxyphenol dissolved in 30 ml of N,N-dimethylformamide, while stirring at room temperature. After stirring at room temperature for 24 hours, the reaction mixture was filtered, and the solvent was removed from the filtrate by distillation under reduced pressure. The residue was subjected to silica gel chromatography, which afforded 9.1 g of 1-(3-bromopropyloxy)4-trifluoromethoxybenzene (60% yield).

후처리

  1. stirringAfter stirring at room temperature for 24 hours
  2. filtrationthe reaction mixture was filtered
  3. customthe solvent was removed from the filtrate by distillation under reduced pressure

출처 및 근거

ORD 기록
ord-6518c9106a434ce08dcee0bb0fcd8727
출처 데이터셋
uspto-grants-1999_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05872137

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