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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 503935Generated: November 3, 2026

Potassium hydroxy sulfite → 3-[4-(2-Cyano-benzenesulfinyl)-2-methoxy-phenyl]-pyrrolidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/503935

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium hydroxy sulfiteHCID 23707502—
Reactant3-[4-(2-Cyano-phenylsulfanyl)-2-methoxy-phenyl]-pyrrolidine-1-carboxylic acid tert-butyl esterHCID 59428429—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product3-[4-(2-Cyano-benzenesulfinyl)-2-methoxy-phenyl]-pyrrolidine-1-carboxylic acid tert-butyl esterHCID 66877134—

Reaction Steps

A solution of OXONE™ (0.470 g, 0.7636 mmol) in water (5 mL) was added to a solution of 3-[4-(2-cyano-phenylsulfanyl)-2-methoxy-phenyl]-pyrrolidine-1-carboxylic acid tert-butyl ester (0.209 g, 0.5091 mmol) in a mixture of MeOH (5 mL) and acetonitrile (5 mL). The reaction mixture was stirred at room temperature for 3 hours, then water was added and the mixture was extracted with EtOAc. The combined organic extracts were washed with water and brine, dried over Na2SO4, filtered, and evaporated under reduced pressure. The resulting crude material was purified via flash chromatography (hexane/EtOAc, 7/3) to give 0.215 g of 3-[4-(2-cyano-benzenesulfinyl)-2-methoxy-phenyl]-pyrrolidine-1-carboxylic acid tert-butyl ester (not shown in Scheme O) as a clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776910B2
Source datasetuspto-grants-2010_08
ORD IDord-d3097b7aa9a34fc6928048ea4c2cf557
Source noteuspto-grants-2010_08