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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1280725Generated: November 2, 2026

HCID 9924295, compound → HCID 69969745, compound

https://huagongshe.com/reaction/1280725

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 9924295HCID 9924295—
ReactantPotassium hydroxy sulfiteHCID 23707502—
SolventMethanolHCID 887—
ProductHCID 69969745HCID 6996974510.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

(2RS,3R)-4-[1-(2-Fluoro-4-phenyl-butyl)-pyrrolidin-3-ylsulfanyl]-phenol (0.56 g, 1.62 mmol) was dissolved in MeOH (50 ml), cooled to 0° C. and treated with oxone (0.5 g, 0.81 mmol). After 4 hours stirring at 0° C., reaction mixture was quenched with saturated NaHCO3 (65 ml). Aqueous phase was extracted with CH2Cl2 (6 times). Combined organic phases were dried over Na2SO4 and the solvent was evaporated. The residue was chromatographed by MPLC over silica gel (CH2Cl2—MeOH, 99:1 then 98:2) then by preparative HPLC (EtOH-heptane, 08:92, detection at 254 nm) to provide (2R,3R, S-oxide R)-4-[1-(2-fluoro-4-phenyl-butyl)-pyrrolidine-3-sulfinyl]-phenol (30 mg, first fraction, 5%), MS: m/e=362.2 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06451819B2
Source datasetuspto-grants-2002_09
ORD IDord-b95285b7f9f449efb71a3b5ce80a85ac
Source noteuspto-grants-2002_09