Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1280726Generated: November 2, 2026

HCID 23381518, compound → HCID 69968980, compound

https://huagongshe.com/reaction/1280726

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 23381518HCID 23381518—
ReactantPotassium hydroxy sulfiteHCID 23707502—
SolventMethanolHCID 887—
ProductHCID 69968980HCID 69968980108.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

(3S)-4-[1-(2,2-Difluoro-4-phenyl-butyl)-pyrrolidin-3-ylsulfanyl]-phenol (0.25 g, 0.688 mmol) was dissolved in MeOH (20 ml), cooled to 0° C. and treated with oxone (0.21 g, 0.34 mmol). After 4 hours stirring at 0° C., reaction mixture was quenched with saturated NaHCO3 (65 ml). Aqueous phase was extracted with CH2Cl2 (3 times). Combined organic phases were dried over Na2SO4 and the solvent was evaporated. The residue was chromatographed by MPLC over silica gel (hexane-ethyl acetate, 98:2 to 50:50) to provide (3S,S-oxide R) or (3S, S-oxide S)-4-[1-(2,2-difluoro-4-phenyl-butyl)-pyrrolidine-3-sulfinyl]-phenol (140 mg, first fraction, 54%), MS: m/e=380.4 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06451819B2
Source datasetuspto-grants-2002_09
ORD IDord-2a9e21de5fd04d7da99947293c1ca36d
Source noteuspto-grants-2002_09