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Hydrochloric Acid → 3-(4-Fluorophenyl)-3-methylbutan-2-one

HRID 1086409
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HRID 1086409 반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](C)([CH3:11])[C:9]#N)=[CH:4][CH:3]=1.C[Li].Cl.C([O:18][CH2:19][CH3:20])C>>[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([CH3:11])([CH3:9])[C:19](=[O:18])[CH3:20])=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 313Hydrochloric AcidHCID 3283Diethyl Ether2회HCID 212511052-(4-Fluorophenyl)-2-methylpropanenitrileHCID 178418348HCID 178418348, 화합물

생성물 1

HCID 198258703-(4-Fluorophenyl)-3-methylbutan-2-one

실험 절차

To a solution of 5.84 g 2-(4-fluorophenyl)-2-methylpropionitrile in abs. diethylether are added dropwise at -30° and under inert gas, 22 ml of a 1.6M solution of methyllithium in diethylether. The cooling bath is then taken away and the mixture stirred for 3 hours at room temperature. The reaction mixture is poured onto ice, the organic phase stirred overnight with 6N HCl, washed after separation of the acid phase, dried and evaporated in vacuum. The thus obtained oily residue is reacted further without purification.

후처리

  1. additionThe reaction mixture is poured onto ice
  2. washwashed
  3. customafter separation of the acid phase
  4. customdried
  5. customevaporated in vacuum
  6. customThe thus obtained oily residue is reacted further without purification

출처 및 근거

ORD 기록
ord-ceda18a4d2a54f94888e9665240f209d
출처 데이터셋
uspto-grants-1991_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05030625

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