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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629751Generated: October 29, 2026

HCID 86726354, compound → HCID 86726353, compound

https://huagongshe.com/reaction/629751

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86726354HCID 86726354—
ReactantHCID 178418676HCID 178418676—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86726353HCID 86726353—

Reaction Conditions

Temperature-40 °C

Reaction Steps

A solution of 4-fluorophenylmagnesium bromide (29 mL of a 2.0 M solution in THF, 58 mmol) and copper(I) bromide-dimethylsulfide complex (12 g, 59 mmol) in THF (100 mL) under an atmosphere of nitrogen was cooled to −40° C. in a dry ice-acetonitrile bath. To the stirred solution was added a solution of (4R)-3-[(2E)-3-(3,5-difluorophenyl)prop-2-enoyl]-4-phenyl-1,3-oxazolidin-2-one (7.7 g, 23 mmol) in 100 mL of THF dropwise over 15 min. The resulting mixture was stirred at −40° C. for 1.5 h, then the cooling bath was removed and the stirred mixture was allowed to warm to ambient temperature. The reaction was quenched by the addition of aqueous NH4Cl solution. The resulting mixture was stirred for 15 min then extracted with two portions of EtOAc. The combined organic phases were washed with water and brine, then dried (MgSO4), filtered, and the solvents were removed in vacuo. The residue was chromatographed on a 330 g SiO2 column using a gradient elution of 0-50% EtOAc:A, where A=1:1 hexanes:CHCl3. Fractions containing product were combined and the solvents were removed in vacuo to give a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315475B2
Source datasetuspto-grants-2016_04
ORD IDord-614fb9de5929485cbecfdda1d5cbcf1b
Source noteuspto-grants-2016_04