Ethyl Acetate → HCID 70981869、化合物

HRID 2280706

反応式

HRID 2280706 の反応式
[C:1]1(=[O:8])[CH2:7][CH2:6][CH2:5][CH2:4][CH:3]=[CH:2]1.[C:9](=[O:16])([O:11][C:12]([CH3:15])([CH3:14])[CH3:13])[NH2:10].O.O.O.O.O.[N+]([O-])([O-])=O.[Bi+3].[N+]([O-])([O-])=O.[N+]([O-])([O-])=O.C(OCC)(=O)C>C(Cl)Cl.O>[O:8]=[C:1]1[CH2:7][CH2:6][CH2:5][CH2:4][CH:3]([NH:10][C:9](=[O:16])[O:11][C:12]([CH3:15])([CH3:14])[CH3:13])[CH2:2]1

参加物

7

実験手順

To a stirring mixture of cyclohept-2-enone (26.96 g, 245.0 mmol) and tert-butyl carbamate (28.7 g, 245 mmol) in DCM (245 mL) was added bismuth nitrate pentahydrate (22.79 g, 47.0 mmol). The resulting mixture was stirred at room temperature overnight. The reaction was diluted reaction with ethyl acetate (500 mL) and water (300 mL) and the biphasic mixture was filtered through a bed of Celite. The bed of Celite was washed well with ethyl acetate and water, and layers of the filtrate separated. The organic layer was concentrated to an oil that was purified by silica gel chromatography (0-40% ethyl acetate in hexanes). Product containing fractions were concentrated to afford the title compound (31.09 g, 137 mmol, 55.9% yield). 1H NMR (400 MHz, DMSO-d6) δ ppm 6.92 (d, J=7.03 Hz, 1H), 3.60 (d, J=8.59 Hz, 1H), 2.55-2.69 (m, 1H), 2.26-2.45 (m, 2H), 1.69-1.93 (m, 3H), 1.44-1.61 (m, 2H), 1.37 (d, J=5.08 Hz, 11H). MS (ESI) m/z 228.5 [M+H]+.

後処理

  1. additionThe reaction was diluted
  2. filtrationthe biphasic mixture was filtered through a bed of Celite
  3. washThe bed of Celite was washed well with ethyl acetate and water, and layers of the filtrate
  4. customseparated
  5. concentrationThe organic layer was concentrated to an oil that
  6. customwas purified by silica gel chromatography (0-40% ethyl acetate in hexanes)
  7. additionProduct containing fractions
  8. concentrationwere concentrated

出典と根拠

ORDレコード
ord-88e9d82919854c128957973d4a1f4bac
出典データセット
uspto-grants-2015_09
特許番号
US09139534B2

関連ノート

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