t-Butyl 5-(6-hydroxymethylpyridin-2-yl)pent-4-ynoate → t-Butyl 5-(6-hydroxymethylpyridin-2-yl)pentanoate

HRID 1172259노트

반응식

HRID 1172259 반응식
[OH:1][CH2:2][C:3]1[N:8]=[C:7]([C:9]#[C:10][CH2:11][CH2:12][C:13]([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:14])[CH:6]=[CH:5][CH:4]=1>[Pt](=O)=O.CCO>[OH:1][CH2:2][C:3]1[N:8]=[C:7]([CH2:9][CH2:10][CH2:11][CH2:12][C:13]([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:14])[CH:6]=[CH:5][CH:4]=1

참가 물질

4

반응물 1

HCID 58105203t-Butyl 5-(6-hydroxymethylpyridin-2-yl)pent-4-ynoate

생성물 1

HCID 58105232t-Butyl 5-(6-hydroxymethylpyridin-2-yl)pentanoate수율 99.2%

시약·촉매·용매 2

HCID 345198Adams' catalyst촉매HCID 702Ethanol용매

실험 절차

To a 200 mL round-bottom flask, 2.76 g of t-butyl 5-(6-hydroxymethylpyridin-2-yl)pent-4-ynoate, 50 mg of platinum dioxide and 25 mL of EtOH were added, the mixture was stirred under hydrogen atmosphere at room temperature for 8 hours. The insoluble material was removed off, and then the filtrate was concentrated to give 2.78 g of t-butyl 5-(6-hydroxymethylpyridin-2-yl)pentanoate as a yellow oil.

후처리

  1. customThe insoluble material was removed off
  2. concentrationthe filtrate was concentrated

출처 및 근거

ORD 기록
ord-b3557cc3c3604bea910fc2c8574264b1
출처 데이터셋
uspto-grants-2010_11
특허 번호
US07834002B2

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