HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 450967Generated: October 25, 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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | (2-Isocyanatocyclopropyl)benzene | HCID 582709 | — |
| Reactant | 1-Chloro-3-phenylhex-5-en-3-ol | HCID 15933475 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 6-Allyl-6-phenyl-3-(2-phenylcyclopropyl)-1,3-oxazinan-2-one | HCID 59532358 | 7.2% |
Reaction Steps
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).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08487094B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-c4483ef8bc41484aa61e4c08c0aa43c2 |
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| Source note | uspto-grants-2013_07 |
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