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2,2-Dimethyl-N-(5-vinylpyridin-2-yl)-propionamide → N-(5-ethylpyridin-2-yl)pivalamide

HRID 1442766
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HRID 1442766 반응식
[CH:1]([C:3]1[CH:4]=[CH:5][C:6]([NH:9][C:10](=[O:15])[C:11]([CH3:14])([CH3:13])[CH3:12])=[N:7][CH:8]=1)=[CH2:2]>CCO.[Pd]>[CH2:1]([C:3]1[CH:4]=[CH:5][C:6]([NH:9][C:10](=[O:15])[C:11]([CH3:14])([CH3:13])[CH3:12])=[N:7][CH:8]=1)[CH3:2]
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참가 물질

4

반응물 1

HCID 217020792,2-Dimethyl-N-(5-vinylpyridin-2-yl)-propionamide

생성물 1

HCID 59272530N-(5-ethylpyridin-2-yl)pivalamide수율 97%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

A catalytic amount of Pd/C was added to a solution of N-(5-vinylpyridin-2-yl)pivalamide (23 g, 0.11 mol) in EtOH (200 mL). The reaction mixture was stirred under hydrogen atmosphere overnight. The catalyst was filtrated off and the solution was concentrated in vacuo to afford N-(5-ethylpyridin-2-yl)pivalamide (22 g, 95%). 1H NMR (CDCl3, 300 MHz) δ 8.15 (d, J=8.4, 1H), 8.09 (d, J=2.4, 1H), 7.96 (br s, 1H), 7.54 (dd, J=8.4 and 2.4, 1H), 2.61 (q, J=7.5, 2H), 1.30 (s, 9 H), 1.23 (t, J=7.5, 3H).

후처리

  1. filtrationThe catalyst was filtrated off
  2. concentrationthe solution was concentrated in vacuo

출처 및 근거

ORD 기록
ord-405eb68871b4408da638233545195055
출처 데이터셋
uspto-grants-2010_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07659268B2

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