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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2037480Generated: November 1, 2026

Hydrochloric Acid → 6-(3-Hydroxypropyl)-6-phenyl-3-(2-phenylcyclopropyl)-1,3-oxazinan-2-one

https://huagongshe.com/reaction/2037480

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHydrogen PeroxideHCID 784—
ReactantSodium HydroxideHCID 14798—
ReactantBorane;tetrahydrofuranHCID 2723981—
Reactant6-Allyl-6-phenyl-3-(2-phenylcyclopropyl)-1,3-oxazinan-2-oneHCID 59532358—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product6-(3-Hydroxypropyl)-6-phenyl-3-(2-phenylcyclopropyl)-1,3-oxazinan-2-oneHCID 59532392—

Reaction Steps

To a solution of 6-allyl-6-phenyl-3-(2-phenylcyclopropyl)-1,3-oxazinan-2-one (200 mg, 0.60 mmol) in dry THF (5 mL) was added dropwise 1 M of BH3/THF (1.8 mL, 1.8 mmol) at 0° C. under N2. After stirring at rt for 2 h, the reaction mixture was cooled to 0° C. again, and water (0.1 mL), 3 M of aqueous NaOH solution (0.1 mL), and 30% H2O2 (0.3 mL) were added sequentially. After the mixture was stirred at rt for another 2 h, 1 N aqueous HCl (0.5 mL) was added. The mixture was extracted with EtOAc. The organic layer was washed with brine, dried over Na2SO4, filtered and concentrated to give the crude product, which was purified by preparative TLC followed by preparative HPLC to afford two isomers.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575156B2
Source datasetuspto-grants-2013_11
ORD IDord-7cea4d82605f4609bd3a4a837d1880ed
Source noteuspto-grants-2013_11