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N-bromobutanimide → (2RS)-1,1,1-trifluoro-2-(4-ethoxyphenyl)-3-[(RS)-alpha-bromo-3-phenoxybenzyloxy]-propane

HRID 483749
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HRID 483749 반응식
[Br:1]N1C(=O)CCC1=O.[F:9][C:10]([F:38])([F:37])[CH:11]([C:28]1[CH:33]=[CH:32][C:31]([O:34][CH2:35][CH3:36])=[CH:30][CH:29]=1)[CH2:12][O:13][CH2:14][C:15]1[CH:20]=[CH:19][CH:18]=[C:17]([O:21][C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)[CH:16]=1>C(Cl)(Cl)(Cl)Cl>[F:9][C:10]([F:37])([F:38])[CH:11]([C:28]1[CH:29]=[CH:30][C:31]([O:34][CH2:35][CH3:36])=[CH:32][CH:33]=1)[CH2:12][O:13][CH:14]([Br:1])[C:15]1[CH:20]=[CH:19][CH:18]=[C:17]([O:21][C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)[CH:16]=1
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참가 물질

4

반응물 2

HCID 67184N-bromobutanimideHCID 106695812-(4-Ethoxyphenyl)-3,3,3-trifluoropropyl 3-phenoxybenzyl ether

생성물 1

HCID 19753527(2RS)-1,1,1-trifluoro-2-(4-ethoxyphenyl)-3-[(RS)-alpha-bromo-3-phenoxybenzyloxy]-propane

시약·촉매·용매 1

HCID 5943Carbon Tetrachloride용매

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온도
0 °C

실험 절차

A catalytic amount of α,α'-azo-iso-butyronitrile was added to a solution of N-bromosuccinimide (0.14 g) and (RS)-1,1,1-trifluoro-2-(4-ethoxyphenyl)-3-(3-phenoxybenzyloxy)propane (0.3 g) in carbon tetrachloride (14 cm3). The reaction mixture was heated at the reflux temperature for 90 minutes, then cooled to 0° C., filtered, and the filtrate concentrated by evaporation under reduced pressure to leave (2RS)-1,1,1-trifluoro-2-(4-ethoxyphenyl)-3-[(RS)-α-bromo-3-phenoxybenzyloxy]-propane as a pale yellow oil which was used without further purification.

후처리

  1. temperatureThe reaction mixture was heated at the reflux temperature for 90 minutes
  2. filtrationfiltered
  3. concentrationthe filtrate concentrated by evaporation under reduced pressure

출처 및 근거

ORD 기록
ord-079204e5cf5f4cfd9c130bd3f8a24d46
출처 데이터셋
uspto-grants-1993_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05225607

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