Water → Benzyl 3-allyl-4-oxocyclopentylcarbamate

HRID 590758

反応式

HRID 590758 の反応式
[CH2:1]=[CH:2][CH2:3][CH:4]1[C:8](=[O:9])[CH:7]=[CH:6][CH2:5]1.[C:10](=[O:20])([O:12][CH2:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)[NH2:11].O.O.O.O.O.[N+]([O-])([O-])=O.[N+]([O-])([O-])=O.[N+]([O-])([O-])=O.[Bi+3].O>ClCCl>[CH2:3]([CH:4]1[C:8](=[O:9])[CH2:7][CH:6]([NH:11][C:10](=[O:20])[O:12][CH2:13][C:14]2[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=2)[CH2:5]1)[CH:2]=[CH2:1]

参加物

6

実験手順

A solution of 5-(propene-3-yl)cyclopent-2-enone (4.28 g, 35 mmol) in dichloromethane (15 mL) was treated with benzyl carbamate (10.6 g, 70 mmol) and bismuth trinitrate pentahydrate (2.2 g, 4.5 mmol), stirred rapidly for 18 h, then diluted with dichloromethane (50 mL). The mixture was filtered through Celite® (rinse with dichloromethane) and the filtrate added directly to a silica gel column (˜550 cc). Elution first with 3:2 petroleum ether/dichloromethane afforded recovered starting material (1.01 g), then 4:1 heptane/ethyl acetate gave the subject compound (4.54 g, 47.5% uncorrected yield) as a pale yellow oil. NMR (CDCl3): δ 7.28 (br s, 5 H), 5.55-5.70 (m, 1 H), 5.03 (br s, 2 H), 4.90-5.10 (m, 2 H), 4.75-4.90 (m, 1 H), 4.10-4.30 (m, 1 H), 2.40-2.80 (m, 2 H), 2.15-2.40 (m, 2 H), 1.85-2.15 (m, 3 H). MS (M+Na): 296.0; MS (M−H2O+1): 256.0 (no M+1 visible).

後処理

  1. filtrationThe mixture was filtered through Celite® (rinse with dichloromethane)
  2. additionthe filtrate added directly to a silica gel column (˜550 cc)
  3. washElution first with 3:2 petroleum ether/dichloromethane
  4. customafforded
  5. customrecovered
  6. custom4:1 heptane/ethyl acetate gave
  7. customthe subject compound (4.54 g, 47.5% uncorrected yield) as a pale yellow oil

出典と根拠

ORDレコード
ord-dbe0b42c5a31407dbb8d7d6ed01b87d4
出典データセット
uspto-grants-2016_01
特許番号
US09233985B2

関連ノート

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