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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1893237Generated: October 31, 2026

Water → HCID 59541970, compound

https://huagongshe.com/reaction/1893237

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl N-(triethylammoniosulfonyl)carbamateHCID 2724994—
ReactantPotassium hydroxy sulfiteHCID 23707502—
ReactantHCID 59541959HCID 59541959—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59541970HCID 59541970—

Reaction Steps

A solution of 4-hydroxy-4-(3-methylsulfanyl-phenyl)-cyclohexanone (as prepared in the previous step, 1.10 g, 4.66 mmol) in THF (10 mL) was treated with Burgess' reagent (1.20 g, 5.00 mmol) at room temperature overnight. The solvent was removed and the residue was partitioned between ethyl acetate and water. The organic layer was washed with brine, dried over anhydrous Na2SO4, filtered, concentrated to give a white solid. To this white solid in MeOH (5 mL) and water (5 mL) was added OXONE (Aldrich, 6.10 g, 10 mmol) at room temperature. The reaction mixture was stirred overnight and quenched with saturated NaHCO3. The solvent was removed in vacuo and the residue was partitioned between ethyl acetate and water. The organic layer was washed with brine, dried over anhydrous Na2SO4, filtered, concentrated and purified by silica gel column on a CombiFlash® system using hexanes and ethyl acetate (from 10% ethyl acetate to 100% ethyl acetate) to afford the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513229B2
Source datasetuspto-grants-2013_08
ORD IDord-75f733aa99dc45a7890b6cefaf5a4347
Source noteuspto-grants-2013_08