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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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tert-Butyl (E)-3-(4-methyl-2-pyridyl)-2-propenoate → tert-Butyl 3-(4-methyl-2-pyridyl)propanoate

HRID 499444
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인쇄 미리보기

반응식

HRID 499444 반응식
[CH3:1][C:2]1[CH:7]=[CH:6][N:5]=[C:4](/[CH:8]=[CH:9]/[C:10]([O:12][C:13]([CH3:16])([CH3:15])[CH3:14])=[O:11])[CH:3]=1>CO.[C].[Pd]>[CH3:1][C:2]1[CH:7]=[CH:6][N:5]=[C:4]([CH2:8][CH2:9][C:10]([O:12][C:13]([CH3:16])([CH3:15])[CH3:14])=[O:11])[CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 23551677tert-Butyl (E)-3-(4-methyl-2-pyridyl)-2-propenoate

생성물 1

HCID 22939611tert-Butyl 3-(4-methyl-2-pyridyl)propanoate수율 95.7%

시약·촉매·용매 2

HCID 178418390HCID 178418390, 화합물촉매HCID 887Methanol용매

실험 절차

tert-Butyl (E)-3-(4-methyl-2-pyridyl)-2-propenoate (1.9 g, 8.5 mmol) was dissolved in methanol (80 ml), and 10% palladium-carbon (200 mg) was added thereto. The mixture was stirred under hydrogen atmosphere at room temperature for 3 hrs. Palladium-carbon was filtered off, and the filtrate was concentrated to give the titled compound (1.8 g, 90%).

후처리

  1. filtrationPalladium-carbon was filtered off
  2. concentrationthe filtrate was concentrated

출처 및 근거

ORD 기록
ord-9dabcc71cd8546a59687f1758a3b6681
출처 데이터셋
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07767665B2

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