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Potassium Cyanide → 1-Benzyl-4-(dimethylamino)piperidine-4-carbonitrile

HRID 2212998
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HRID 2212998 반응식
[C:1]1([CH2:7][N:8]2[CH2:13][CH2:12][C:11](=O)[CH2:10][CH2:9]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[C-:15]#[N:16].[K+].Cl.[CH3:19][NH:20][CH3:21]>C(O)C.O>[CH3:19][N:20]([CH3:21])[C:11]1([C:15]#[N:16])[CH2:12][CH2:13][N:8]([CH2:7][C:1]2[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=2)[CH2:9][CH2:10]1
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참가 물질

6

반응물 3

HCID 9032Potassium CyanideHCID 10473Dimethylamine, hydrochlorideHCID 192201-Benzyl-4-piperidone

생성물 1

HCID 164539151-Benzyl-4-(dimethylamino)piperidine-4-carbonitrile수율 96.1%

시약·촉매·용매 2

HCID 702Ethanol용매HCID 962Water용매2회

실험 절차

A solution of 1-(phenylmethyl)-4-piperidone (9.46 g, 50 mmol) in ethanol (20 mL) was added slowly to a stirred solution of potassium cyanide (3.58 g, 55 mmol) and dimethylamine hydrochloride (4.89 g, 60 mmol) in water (60 mL). The mixture was stirred at room temperature for 68 hours, then water (100 mL) was added. The solid was collected, suspended in aqueous sodium hydrogen carbonate (saturated, 100 mL) and water (50 mL) and extracted with dichloromethane (3×100 mL). The combined organic fractions were dried (MgSO4) and the solvent was evaporated under reduced pressure to give the the title compound as a cream solid (11.69 g, 96%). m/z (ES+) 244 (M+1).

후처리

  1. customThe solid was collected
  2. extractionwater (50 mL) and extracted with dichloromethane (3×100 mL)
  3. dry with materialThe combined organic fractions were dried (MgSO4)
  4. customthe solvent was evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-291adae48e0342db817d4c15949f9bac
출처 데이터셋
uspto-grants-2006_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07105507B2

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