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Methyl 4-[3-(3-benzyloxy-2-pyridyl)prop-2-enyl]benzoate → Methyl 4-[3-(3-hydroxy-2-pyridyl)propyl]benzoate

HRID 2395077
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인쇄 미리보기

반응식

HRID 2395077 반응식
C([O:8][C:9]1[C:10]([CH:15]=[CH:16][CH2:17][C:18]2[CH:27]=[CH:26][C:21]([C:22]([O:24][CH3:25])=[O:23])=[CH:20][CH:19]=2)=[N:11][CH:12]=[CH:13][CH:14]=1)C1C=CC=CC=1>C(O)C.CCOC(C)=O.[Pd]>[OH:8][C:9]1[C:10]([CH2:15][CH2:16][CH2:17][C:18]2[CH:27]=[CH:26][C:21]([C:22]([O:24][CH3:25])=[O:23])=[CH:20][CH:19]=2)=[N:11][CH:12]=[CH:13][CH:14]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 1

HCID 54508749Methyl 4-[3-(3-benzyloxy-2-pyridyl)prop-2-enyl]benzoate

생성물 1

HCID 18974066Methyl 4-[3-(3-hydroxy-2-pyridyl)propyl]benzoate수율 77.2%

시약·촉매·용매 3

HCID 23938Palladium촉매HCID 702Ethanol용매HCID 8857Ethyl Acetate용매

실험 절차

Methyl 4-[3-(3-benzyloxy-2-pyridyl)prop-2-enyl]benzoate (1.5 g, 4.2 mmol) was dissolved in ethanol (5 ml) and EtOAc (15 ml), treated with 10% palladium on carbon (0.15 g) and placed under a hydrogen atmosphere. The mixture was stirred at ambient temperature for 10 hours and filtered and evaporated to give methyl 4-[3-(3-hydroxy-2-pyridyl)propyl]benzoate as a yellow oil (0.88 g, 77%).

후처리

  1. filtrationfiltered
  2. customevaporated

출처 및 근거

ORD 기록
ord-5f873da4a15f4cd8b3bf0753b4f869d3
출처 데이터셋
uspto-grants-1998_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05811459

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