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2-(trimethylsilyl)ethyl 4-oxo-2-vinyl-3,4-dihydropyridine-1(2H)-carboxylate → 2-(Trimethylsilyl)ethyl 4-oxo-2-vinylpiperidine-1-carboxylate

HRID 1510157
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인쇄 미리보기

반응식

HRID 1510157 반응식
[O:1]=[C:2]1[CH:7]=[CH:6][N:5]([C:8]([O:10][CH2:11][CH2:12][Si:13]([CH3:16])([CH3:15])[CH3:14])=[O:9])[CH:4]([CH:17]=[CH2:18])[CH2:3]1>C(O)(=O)C.[Zn]>[O:1]=[C:2]1[CH2:7][CH2:6][N:5]([C:8]([O:10][CH2:11][CH2:12][Si:13]([CH3:16])([CH3:15])[CH3:14])=[O:9])[CH:4]([CH:17]=[CH2:18])[CH2:3]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 667907952-(trimethylsilyl)ethyl 4-oxo-2-vinyl-3,4-dihydropyridine-1(2H)-carboxylate

생성물 1

HCID 667904002-(Trimethylsilyl)ethyl 4-oxo-2-vinylpiperidine-1-carboxylate

시약·촉매·용매 2

HCID 23994Zinc촉매HCID 176Acetic Acid용매

실험 절차

2-(trimethylsilyl)ethyl 4-oxo-2-vinyl-3,4-dihydropyridine-1(2H)-carboxylate (29.1 g, 109 mmol) in acetic acid (500 ml) was added zinc dust (42.7 g, 652 mmol). The solution stirred at room temperature for 2 hrs and was filtered through a pad of celite. The solvent was evaporated under reduced pressure and the product was purified by column chromatography on silica gel Biotage 65i, eluting with 20% ethyl acetate/hexanes.

후처리

  1. filtrationwas filtered through a pad of celite
  2. customThe solvent was evaporated under reduced pressure
  3. customthe product was purified by column chromatography on silica gel Biotage 65i
  4. washeluting with 20% ethyl acetate/hexanes

출처 및 근거

ORD 기록
ord-be60c7eb4b2c4fbb9f2843eb49cfc8db
출처 데이터셋
uspto-grants-2012_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08211904B2

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