Water → Benzyl 3-allyl-4-oxocyclopentylcarbamate

HRID 61413

Reaktionsgleichung

Reaktionsgleichung von HRID 61413
[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]

Komponenten

6

Edukt 4

HCID 962WaterHCID 12136Benzyl carbamateHCID 160911Bismuth nitrate pentahydrateHCID 134445455-(Prop-2-en-1-yl)cyclopent-2-en-1-one

Produkt 1

HCID 67513633Benzyl 3-allyl-4-oxocyclopentylcarbamate

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel2×

Versuchsvorschrift

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).

Aufarbeitung

  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

Quellen und Nachweise

ORD-Eintrag
ord-f2d56955c2bc4d60b6aa20377463e990
Quelldatensatz
uspto-grants-2016_09
Patentnummer
US09440995B2

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