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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 863586Generated: October 30, 2026

Methanol → HCID 53856125, compound

https://huagongshe.com/reaction/863586

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
ReactantPotassium hydroxy sulfiteHCID 23707502—
ReactantHCID 70197397HCID 70197397—
SolventWaterHCID 962—
ProductHCID 53856125HCID 53856125—

Reaction Steps

To a stirred and ice-cooled solution of (2S,3S)-N-(2-methoxy-5-methylthiophenyl)methyl-2-diphenylmethyl-1-azabicyclo[2.2.2]octan-3-amine dihydrochloride in methanol (25 mL) was added a solution of oxone (2.41 g) in water (25 mL). The reaction mixture was stirred at room temperature for 2.5 hours. The reaction mixture was basified to pH 10-11 with 1N NaOH aq. solution with ice-cooling, and extracted with CHCl3 (80 mL×4). The combined organic layers were washed with brine (80 mL), dried (MgSO4) and concentrated in vacuo to give crude (2S,3S)-N-(2-methoxy-5-methylsulfonylphenyl)methyl-2-diphenylmethyl-1-azabicyclo[2.2.2]octan-3-amine (white soap, 1.49 g). The residue was purified by chromatography on silica gel (60 g) with chloroform-methanol (20:1-10:1) to give (2S,3S)-N-(2-methoxy-5-methylsulfonylphenyl)methyl-2-diphenylmethyl-1-azabicyclo[2.2.2]octan-3-amine (1.08 g, 79%) as a white amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05721255
Source datasetuspto-grants-1998_02
ORD IDord-8e77e35b39c1468cab18fe7c5d5d7749
Source noteuspto-grants-1998_02