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Nitromethane → 4-Hydroxy-4-nitromethyl-1-(4-pyridyl)piperidine

HRID 1244797
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반응식

HRID 1244797 반응식
[N+:1]([CH3:4])([O-:3])=[O:2].[Na].[N:6]1[CH:11]=[CH:10][C:9]([N:12]2[CH2:17][CH2:16][C:15](=[O:18])[CH2:14][CH2:13]2)=[CH:8][CH:7]=1>CO>[OH:18][C:15]1([CH2:4][N+:1]([O-:3])=[O:2])[CH2:14][CH2:13][N:12]([C:9]2[CH:8]=[CH:7][N:6]=[CH:11][CH:10]=2)[CH2:17][CH2:16]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6375NitromethaneHCID 5360545SodiumHCID 113327931-(Pyridin-4-yl)piperidin-4-one

생성물 1

HCID 219225514-Hydroxy-4-nitromethyl-1-(4-pyridyl)piperidine

시약·촉매·용매 1

HCID 887Methanol용매2회

실험 절차

To a solution of nitromethane (2.31 ml) in methanol (5.4 ml) was added sodium (70 mg) at ice-cooled temperature. The resulting mixture was added dropwise to a solution of 1-(4-pyridyl)-4-piperidone (5.36 g) in methanol (10.7 ml) at ice-cooled temperature for 10 minutes, and stirred for 15 hours at room temperature. The precipitate was filtered, and washed with methanol to obtain the title compound (5.31 g).

후처리

  1. temperaturecooled temperature
  2. temperaturecooled temperature for 10 minutes
  3. filtrationThe precipitate was filtered
  4. washwashed with methanol

출처 및 근거

ORD 기록
ord-d9599f7173324e9ea78140f997f09029
출처 데이터셋
uspto-grants-2006_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07122662B2

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