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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640780Generated: October 30, 2026

(S)-3-((S)-1-(4-bromophenyl)ethyl)-6-(2-oxopropyl)-6-phenyl-1,3-oxazinan-2-one → 6-(2-Hydroxy-2-methylpropyl)-6-phenyl-1,3-oxazinan-2-one

https://huagongshe.com/reaction/1640780

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-3-((S)-1-(4-bromophenyl)ethyl)-6-(2-oxopropyl)-6-phenyl-1,3-oxazinan-2-oneHCID 59532378—
ReactantHCID 178418573HCID 178418573—
SolventTetrahydrofuranHCID 8028—
Product6-(2-Hydroxy-2-methylpropyl)-6-phenyl-1,3-oxazinan-2-oneHCID 8664975791.9%

Reaction Steps

To a solution of (S)-3-((S)-1-(4-bromophenyl)ethyl)-6-(2-oxopropyl)-6-phenyl -1,3-oxazinan-2-one (12 g, 28.8 mmol) in anhydrous THF (100 mL) was added dropwise methylmagnesium bromide (48 mL, 144 mmol) at −78° C. under nitrogen. The mixture was stirred at rt for 1 h. The reaction mixture was quenched with aqueous NH4Cl solution (50 mL) in ice water bath. The layers were separated and the aqueous layer was extracted with EtOAc (150 mL). The combined organic phases were washed with brine (30 mL), dried over Na2SO4 and concentrated in vacuo to give the crude product, which was purified by preparative HPLC and chiral HPLC to afford (S)-3-(S)-1-(4-bromophenyl)ethyl)-6-(2-hydroxy-2-methylpropyl)-6-phenyl-1,3-oxazinan-2-one (6.6 g, 53%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08114868B2
Source datasetuspto-grants-2012_02
ORD IDord-8f6886dbad314d3dbb552f394af4316b
Source noteuspto-grants-2012_02