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Acetic Acid → 4-(piperidin-1-ylmethyl)benzonitrile

HRID 1191003
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HRID 1191003 반응식
C([BH3-])#N.[Na+].[C:5]([C:7]1[CH:14]=[CH:13][C:10]([CH:11]=O)=[CH:9][CH:8]=1)#[N:6].[NH:15]1[CH2:20][CH2:19][CH2:18][CH2:17][CH2:16]1.C(O)(=O)C>CO>[N:15]1([CH2:11][C:10]2[CH:13]=[CH:14][C:7]([C:5]#[N:6])=[CH:8][CH:9]=2)[CH2:20][CH2:19][CH2:18][CH2:17][CH2:16]1
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참가 물질

6

반응물 4

HCID 176Acetic AcidHCID 8082PiperidineHCID 660424-CyanobenzaldehydeHCID 5003444Sodium cyanoborohydride

생성물 1

HCID 75376034-(piperidin-1-ylmethyl)benzonitrile수율 54.1%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

Under a nitrogen atmosphere, add sodium cyanoborohydride (5.77 g, 91.6 mmol) to a solution of 4-cyanobenzaldehyde (3 g, 22.9 mmol), piperidine (5.84 g, 68.7 mmol) and acetic acid (2.75 g, 45.8 mmol) in methanol (30 mL) at 0° C. with stirring. Warm the mixture to room temperature and stir overnight. Add water (100 mL), saturated aqueous K2CO3 (50 mL), and extract with DCM. Wash the combined organic extracts with water and brine. Dry the organic phase over Na2SO4, filter, and concentrate in vacuo. Purify by chromatography on silica gel (400 g) eluting with hexane/EtOAc (1:0 to 4:1 gradient) to obtain the desired intermediate as a clear oil (2.48 g, 54%). MS (APCI+) m/z: 201 (M+H)+.

후처리

  1. stirringstir overnight
  2. extractionAdd water (100 mL), saturated aqueous K2CO3 (50 mL), and extract with DCM
  3. washWash the combined organic extracts with water and brine
  4. dry with materialDry the organic phase over Na2SO4
  5. filtrationfilter
  6. concentrationconcentrate in vacuo
  7. customPurify by chromatography on silica gel (400 g)
  8. washeluting with hexane/EtOAc (1:0 to 4:1 gradient)

출처 및 근거

ORD 기록
ord-67f9a992c6344b3bac0d680cfafb51b6
출처 데이터셋
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08680091B2

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