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Piperidine → 2-Methyl-1-(4-(piperidin-1-yl)phenyl)propan-1-one

HRID 981753
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HRID 981753 반응식
F[C:2]1[CH:7]=[CH:6][C:5]([C:8](=[O:12])[CH:9]([CH3:11])[CH3:10])=[CH:4][CH:3]=1.C(Cl)(=O)C(C)C.FC1C=CC=CC=1.[NH:26]1[CH2:31][CH2:30][CH2:29][CH2:28][CH2:27]1.C(=O)([O-])[O-].[K+].[K+]>CS(C)=O>[CH3:10][CH:9]([CH3:11])[C:8]([C:5]1[CH:6]=[CH:7][C:2]([N:26]2[CH2:31][CH2:30][CH2:29][CH2:28][CH2:27]2)=[CH:3][CH:4]=1)=[O:12]
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참가 물질

7

반응물 5

HCID 8082PiperidineHCID 10008FluorobenzeneHCID 11430Potassium CarbonateHCID 62325Isobutyryl chlorideHCID 27828291-(4-Fluorophenyl)-2-methylpropan-1-one

생성물 1

HCID 212571912-Methyl-1-(4-(piperidin-1-yl)phenyl)propan-1-one

시약·촉매·용매 1

HCID 679
Dimethyl Sulfoxide
용매

반응 조건

온도
110 °C

실험 절차

49.86 (0.30 mol) of 1-(4-fluorophenyl)-2-methylpropan-1-one, prepared by a Friedel-Crafts reaction from isobutyryl chloride with fluorobenzene analogously to European Patent Application No. 3,002, and 25.5 g (0.30 mol) of piperidine are dissolved in 120 ml of dimethyl sulfoxide, and the solution is heated to 110° C. together with 41.5 g (0.30 mol) of potassium carbonate. After 16 hours of stirring at 110° C. the suspension is cooled down and is poured onto an ice-water mixture. The crystals are filtered off, are washed with water and are recrystallised from hexane.

후처리

  1. temperatureis cooled down
  2. filtrationThe crystals are filtered off
  3. washare washed with water
  4. customare recrystallised from hexane

출처 및 근거

ORD 기록
ord-60e72f52f6ba490586c066d66c9515a9
출처 데이터셋
uspto-grants-1991_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04992547

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