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Potassium Carbonate → [4-(3-Methoxyphenyl)-1-piperidinyl]acetonitrile

HRID 611483
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반응식

HRID 611483 반응식
Br[CH2:2][C:3]#[N:4].[CH3:5][O:6][C:7]1[CH:8]=[C:9]([CH:13]2[CH2:18][CH2:17][NH:16][CH2:15][CH2:14]2)[CH:10]=[CH:11][CH:12]=1.C([O-])([O-])=O.[K+].[K+]>CC#N>[CH3:5][O:6][C:7]1[CH:8]=[C:9]([CH:13]2[CH2:18][CH2:17][N:16]([CH2:2][C:3]#[N:4])[CH2:15][CH2:14]2)[CH:10]=[CH:11][CH:12]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 11430Potassium CarbonateHCID 11534BromoacetonitrileHCID 107028904-(3-Methoxyphenyl)piperidine

생성물 1

HCID 19597357[4-(3-Methoxyphenyl)-1-piperidinyl]acetonitrile수율 97%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

A mixture of bromoacetonitrile (0.70 mL, 10 mmol), 4-(3-methoxyphenyl)piperidine (1.74 g, 9.1 mmol) and K2CO3 (1.3 g) in MeCN was stirred at room temperature for 3 days. The reaction mixture was partitioned between CH2Cl2 and H2O, and the organic extract was dried (Na2SO4). The solvent was then removed in vacuo to afford [4-(3-methoxyphenyl)-1-piperidinyl]acetonitrile as an amber oil (2.03 g, 97%): MS (DCl) m/z 231 (MH+). Anal. Calcd. for C14H18N2O.0.5 H2O: C, 70.27; H, 8.00; N, 11.71. Found: C, 70.12; H, 7.67; N, 11.87.

후처리

  1. customThe reaction mixture was partitioned between CH2Cl2 and H2O
  2. extractionthe organic extract
  3. dry with materialwas dried (Na2SO4)
  4. customThe solvent was then removed in vacuo

출처 및 근거

ORD 기록
ord-b10a7b1104084050927bdf1883e6972d
출처 데이터셋
uspto-grants-1999_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06001836

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