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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1383785Generated: October 31, 2026

Hexane → (4S,5R)-4-(3,4-difluorophenyl)-5-(tetrahydropyran-2-yloxymethyl)-oxazolidin-2-one

https://huagongshe.com/reaction/1383785

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
Reactant3,4-dihydro-2H-pyranHCID 8080—
ReactantEthyl AcetateHCID 8857—
Reactant(4S,5R) 4-(3,4-difluorophenyl)-5-hydroxymethyl-oxazolidin-2-oneHCID 57254260—
SolventDichloromethaneHCID 6344—
Product(4S,5R)-4-(3,4-difluorophenyl)-5-(tetrahydropyran-2-yloxymethyl)-oxazolidin-2-oneHCID 5708111480%

Reaction Steps

To a solution of (4S,5R) 4-(3,4-difluorophenyl)-5-hydroxymethyl-oxazolidin-2-one (695 mg, 3.0 mmol) in dry dichloromethane (30 mL) was added 2,3-dihydropyran (0.3 mL, 3.6 mmol) and cam phorsulfonic acid (70 mg, 0.3 mmol). The reaction mixture was stirred at ambient temperature for 3 h. The reaction mixture was diluted with dichloromethane (100 mL) and washed with saturated sodium bicarbonate solution (2×100 ml), brine (1×100 ml), dried over magnesium sulfate and filtered. The volatiles were removed under reduced pressure and the resulting solid was purified by pressurized silica gel chromatography (1:1 then 2:1 ethyl acetate:hexane) to afford (4S,5R)-4-(3,4-difluorophenyl)-5-(tetrahydropyran-2-yloxymethyl)-oxazolidin-2-one as a colorless oil (750 mg, 2.4 mmol, 80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06255315B1
Source datasetuspto-grants-2001_07
ORD IDord-9332d9c3b5d742389590a174681aadd0
Source noteuspto-grants-2001_07