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N-bromobutanimide → 1-(Bromomethyl)-4-(1,1,2,2-tetrafluoroethoxy)benzene

HRID 1610262
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HRID 1610262 반응식
[F:1][C:2]([F:14])([O:6][C:7]1[CH:12]=[CH:11][C:10]([CH3:13])=[CH:9][CH:8]=1)[CH:3]([F:5])[F:4].[Br:15]N1C(=O)CCC1=O>C(Cl)(Cl)(Cl)Cl>[F:1][C:2]([F:14])([O:6][C:7]1[CH:12]=[CH:11][C:10]([CH2:13][Br:15])=[CH:9][CH:8]=1)[CH:3]([F:4])[F:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 67184N-bromobutanimideHCID 744394-(1,1,2,2-Tetrafluoroethoxy)toluene

생성물 1

HCID 222617841-(Bromomethyl)-4-(1,1,2,2-tetrafluoroethoxy)benzene

시약·촉매·용매 1

HCID 5943Carbon Tetrachloride용매

실험 절차

A solution of 4-(1,1,2,2-tetrafluoroethoxy)toluene (6.73 g, 32.3 mmol), N-bromosuccinimide (5.75 g, 32.3 mmol) and 2,2-azobis(isobutyronitrile) (0.2 g) in carbon tetrachloride (30 ml) was heated under reflux for 0.5 hr. After cooling the reaction solution to room temperature, the white precipitate as removed by filtration and the precipitate was washed with diethyl ether. The solvent of the collected filtrate was evaporated under reduced pressure to give a crude product of 4-(1,1,2,2-tetrafluoroethoxy)benzyl bromide as a pale-yellow liquid.

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후처리

  1. temperatureunder reflux for 0.5 hr
  2. customthe white precipitate as removed by filtration
  3. washthe precipitate was washed with diethyl ether
  4. customThe solvent of the collected filtrate was evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-cb18a0d76d044ff894102acc3746e80d
출처 데이터셋
uspto-grants-2006_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06982348B2

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