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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640724Generated: November 1, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → 6-(4-Fluorophenyl)-6-(2-methylallyl)-1,3-oxazinan-2-one

https://huagongshe.com/reaction/1640724

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant1-Chloro-3-(4-fluorophenyl)-5-methylhex-5-en-3-olHCID 59635674—
Reactant(S)-(-)-1-(-bromophenyl)ethyl isocyanateHCID 86649409—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product6-(4-Fluorophenyl)-6-(2-methylallyl)-1,3-oxazinan-2-oneHCID 8664940865.7%

Reaction Steps

A mixture of 1-chloro-3-(4-fluorophenyl)-5-methylhex-5-en-3-ol (3.15 g, 13 mmol), (S)-(−)-1-(-bromophenyl)ethyl isocyanate (3.5 g, 16 mmol), and DBU (8 g, 33 mmol) in THF (80 mL) was heated to reflux for 25 h. The mixture was diluted with EtOAc and washed with 1 N aq HCl. The aqueous phase was extracted with EtOAc (3 x). The combined organic phase was dried over Na2SO4. After the solvents were evaporated, the crude product was purified by column to give (R)-3-(S)-1-(4-bromophenyl)-ethyl)-6-(4-fluorophenyl)-6-(2-methylallyl)-1,3-oxazinan-2-one (2.13 g, yield: 38%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08114868B2
Source datasetuspto-grants-2012_02
ORD IDord-9581f43c9722405aaf02ed7f6f8f4ef0
Source noteuspto-grants-2012_02