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Water → 1-(2-Chloroacetyl)piperidine-4-carbonitrile

HRID 1023020
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HRID 1023020 반응식
[Cl:1][CH2:2][C:3]([N:5]1[CH2:10][CH2:9][CH:8]([C:11]([NH:13]C(C)(C)C)=O)[CH2:7][CH2:6]1)=[O:4].P(Cl)(Cl)(Cl)=O.O.[OH-].[Na+]>CN(C)C=O>[Cl:1][CH2:2][C:3]([N:5]1[CH2:6][CH2:7][CH:8]([C:11]#[N:13])[CH2:9][CH2:10]1)=[O:4]
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참가 물질

6

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HCID 962WaterHCID 14798Sodium HydroxideHCID 24813Phosphorus oxychlorideHCID 687433101-(2-chloroacetyl)-N-(1,1-dimethylethyl)-4-piperidinecarboxamide

생성물 1

HCID 674700971-(2-Chloroacetyl)piperidine-4-carbonitrile수율 97%

시약·촉매·용매 1

HCID 6228
Dimethylformamide
용매

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온도
55 °C

실험 절차

To a solution of 1-(2-chloroacetyl)-N-(1,1-dimethylethyl)-4-piperidinecarboxamide (26.1 g, 0.10 mol) in N,N-dimethylformamide (35 mL) was added phosphorus oxychloride (18.8 g, 0.123 mol) dropwise over 30 minutes while allowing the temperature of the reaction mixture to rise to 37° C. The reaction mixture was heated at 55° C. for 1 h and then was slowly added to water (about 150 g) cooled with ice to maintain a temperature of about 10° C. The pH of the reaction mixture was adjusted to 5.5 with 50% NaOH aqueous solution. The mixture was extracted with dichloromethane (4×100 mL), and the combined extract was concentrated under reduced pressure to give 18.1 g of the title compound as a solid. This compound was of sufficient purity to use in subsequent reactions.

후처리

  1. customto rise to 37° C
  2. temperaturecooled with ice
  3. temperatureto maintain a temperature of about 10° C
  4. extractionThe mixture was extracted with dichloromethane (4×100 mL)
  5. extractionthe combined extract
  6. concentrationwas concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-b4a7b5c27f034d09b3dc1da4837bd01d
출처 데이터셋
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08722678B2

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