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Benzoyl Peroxide → HCID 46938920, 화합물

HRID 2106013
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HRID 2106013 반응식
[Br:1]N1C(=O)CCC1=O.C(OOC(=O)C1C=CC=CC=1)(=O)C1C=CC=CC=1.[F:27][C:28]([F:44])([F:43])[C:29](=[O:42])[CH2:30][C:31]([C:34]1[CH:39]=[CH:38][CH:37]=[CH:36][C:35]=1[O:40][CH3:41])([CH3:33])[CH3:32]>C(Cl)(Cl)(Cl)Cl>[F:27][C:28]([F:43])([F:44])[C:29](=[O:42])[CH2:30][C:31]([C:34]1[CH:39]=[C:38]([Br:1])[CH:37]=[CH:36][C:35]=1[O:40][CH3:41])([CH3:33])[CH3:32]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7187Benzoyl PeroxideHCID 67184N-bromobutanimideHCID 46938919HCID 46938919, 화합물

생성물 1

HCID 46938920HCID 46938920, 화합물

시약·촉매·용매 1

HCID 5943Carbon Tetrachloride용매

실험 절차

A mixture of N-bromosuccinimide (6.84 g, 38.42 mmol), benzoylperoxide (catalytic amount) and 1,1,1-trifluoro-4-(2-methoxyphenyl)-4-methylpentan-2-one (10.0 g, 38.42 mmol) in carbon tetrachloride (120 mL) and was refluxed for two days. After cooling, the solution was washed with water (60 mL) and 1.0M NaOH (60 mL), dried over sodium sulfate (Na2SO4), and concentrated in vacuo giving 1,1,1-trifluoro-4-(5-bromo-2-methoxyphenyl)-4-methylpentan-2-one and the starting material as 3:1 mixture (13.0 g).

후처리

  1. temperaturewas refluxed for two days
  2. temperatureAfter cooling
  3. washthe solution was washed with water (60 mL) and 1.0M NaOH (60 mL)
  4. dry with materialdried over sodium sulfate (Na2SO4)
  5. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-d8ce9b4f5c0e42a193799bac71390335
출처 데이터셋
uspto-grants-2009_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07579469B2

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