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4-Hydroxymethyl-1-(3-chlorophenyl)-1H-pyridin-2-one → 1-(3-Chloro-phenyl)-2-oxo-1,2-dihydro-pyridine-4-carbaldehyde

HRID 2289641
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인쇄 미리보기

반응식

HRID 2289641 반응식
[OH:1][CH2:2][C:3]1[CH:8]=[CH:7][N:6]([C:9]2[CH:14]=[CH:13][CH:12]=[C:11]([Cl:15])[CH:10]=2)[C:5](=[O:16])[CH:4]=1>C(Cl)Cl.O=[Mn]=O>[Cl:15][C:11]1[CH:10]=[C:9]([N:6]2[CH:7]=[CH:8][C:3]([CH:2]=[O:1])=[CH:4][C:5]2=[O:16])[CH:14]=[CH:13][CH:12]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 186987734-Hydroxymethyl-1-(3-chlorophenyl)-1H-pyridin-2-one

생성물 1

HCID 186987831-(3-Chloro-phenyl)-2-oxo-1,2-dihydro-pyridine-4-carbaldehyde

시약·촉매·용매 2

HCID 14801Manganese dioxide촉매HCID 6344Dichloromethane용매

실험 절차

To a solution of 4-hydroxymethyl-1-(3-chlorophenyl)-1H-pyridin-2-one (2.39 g, 10.14 mmol) in CH2Cl2 (250 ml) was added MnO2 (4.41 g, 50.71 mmol) and stirred for 18 hours. The suspension was filtered through celite and the pad washed with additional CH2Cl2 (200 ml). The combined filtrates were evaporated in vacuo and chromatographed (silica gel, 5-20% EtOAc: CH2Cl2 gradient elution) to afford the title compound.

후처리

  1. filtrationThe suspension was filtered through celite
  2. washthe pad washed with additional CH2Cl2 (200 ml)
  3. customThe combined filtrates were evaporated in vacuo
  4. customchromatographed
  5. wash(silica gel, 5-20% EtOAc: CH2Cl2 gradient elution)

출처 및 근거

ORD 기록
ord-8092fa023ba84a0997d2cb42ad3da008
출처 데이터셋
uspto-grants-2000_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06093737

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