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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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1-(4-Bromophenyl)propan-2-one → 1-(4-Bromophenyl)-2-methylpropan-2-ol

HRID 2223054
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HRID 2223054 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:9](=[O:11])[CH3:10])=[CH:4][CH:3]=1.[CH3:12][Mg]Br>C(OCC)C>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:8][C:9]([CH3:12])([OH:11])[CH3:10])=[CH:6][CH:7]=1
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참가 물질

4

반응물 2

HCID 7363321-(4-Bromophenyl)propan-2-oneHCID 178418573HCID 178418573, 화합물

생성물 1

HCID 3167851-(4-Bromophenyl)-2-methylpropan-2-ol수율 84%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매2회

실험 절차

A solution of 4-bromophenylacteone (6.85 g, 32 mmol) in diethyl-ether (100 ml) was cooled to 0° C. and treated with methylmagnesium bromide (23.5 ml of a 3M solution in diethyl-ether, 70 mmol). The reaction mixture was allowed to warm gradually to room temperature. After 2 hours the reaction was quenched by addition of saturated aqueous ammonium chloride (200 ml). The organic phase was separated and washed with saturated sodium chloride (100 ml), dried (sodium sulfate) and reduced in vacuo. Purification by flash column chromatography on silica gel eluting with pentane:dichloromethane (60:40 changing to 0:100, by volume) gave the title compound as a colourless oil (6.23 g, 84%).

후처리

  1. customAfter 2 hours the reaction was quenched by addition of saturated aqueous ammonium chloride (200 ml)
  2. customThe organic phase was separated
  3. washwashed with saturated sodium chloride (100 ml)
  4. dry with materialdried (sodium sulfate)
  5. customPurification by flash column chromatography on silica gel eluting with pentane:dichloromethane (60:40 changing to 0:100, by volume)

출처 및 근거

ORD 기록
ord-041b0b648ccd4818976879baba8772b3
출처 데이터셋
uspto-grants-2008_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07375100B2

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