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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 450967Erstellt: 27. Oktober 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → 6-Allyl-6-phenyl-3-(2-phenylcyclopropyl)-1,3-oxazinan-2-one

https://huagongshe.com/reaction/450967

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Edukt(2-Isocyanatocyclopropyl)benzeneHCID 582709—
Edukt1-Chloro-3-phenylhex-5-en-3-olHCID 15933475—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
Produkt6-Allyl-6-phenyl-3-(2-phenylcyclopropyl)-1,3-oxazinan-2-oneHCID 595323587,2%

Reaktionsschritte

To a solution of (2-isocyanatocyclopropyl)benzene (800 mg, 5.03 mmol) in THF (15 mL) was added DBU (1.61 g, 10.48 mmol) and 1-chloro-3-phenylhex-5-en-3-ol (880 mg, 4.19 mmol), and the mixture was refluxed overnight. The solution was diluted with EtOAc, and washed with 1 N HCl (2×15 mL). The aqueous phase was extracted with EtOAc. The combined organic layers were washed with brine, dried over Na2SO4, filtered and concentrated to give crude product, which was purified by preparative TLC to afford 6-allyl-6-phenyl-3-(2-phenylcyclopropyl)-1,3-oxazinan-2-one (100 mg, 6%). 1H NMR (CDCl3): 1.05-1.21 (m, 3H), 1.36-1.42 (m, 1H), 2.13-2.34 (m, 1H), 2.39-2.61 (m, 2H), 2.92-3.15 (m, 1H), 3.76-4.01 (m, 1H), 4.95-5.10 (m, 2H), 5.42-5.73 (m, 1H), 6.95-6.99 (m, 1H), 7.10-7.24 (m, 10H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08487094B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-c4483ef8bc41484aa61e4c08c0aa43c2
Quellennotizuspto-grants-2013_07