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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2221303Generated: November 3, 2026

Potassium Hydroxide → (7-benzenesulfonyl-2,3-dihydro-benzo[1,4]dioxin-2(R)-yl)-methanol

https://huagongshe.com/reaction/2221303

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant1-(5-benzenesulfonyl-2-(S)-oxiranylmethoxy-phenyl)-ethanoneHCID 86601557—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
Product(7-benzenesulfonyl-2,3-dihydro-benzo[1,4]dioxin-2(R)-yl)-methanolHCID 59710879—

Reaction Steps

A solution of 1-(5-benzenesulfonyl-2-(S)-oxiranylmethoxy-phenyl)-ethanone (2.04 g; 0.059 mol) and meta-chloroperoxybenzoic acid (4.13 g; 0.018 mol, max. 77%) in chloroform (20 mL) was heated under reflux for 18 hours. After cooling to ambient temperature the mixture was diluted with chloroform, filtered, washed with water and saturated sodium bicarbonate, dried (Na2SO4) and concentrated in vacuo. This crude residue (0.85 g; 0.0024 mol) dissolved in methanol (5 mL) was added to a solution of 10% aqueous potassium hydroxide (4 mL) at 0° C. The mixture was stirred for 30 minutes at room temperature. Solvent was removed in vacuo, and the residue was dissolve in ethyl acetate, washed with 10% aqueous hydrochloric acid followed by saturated brine, dried (Na2SO4) and concentrated in vacuo to give (7-benzenesulfonyl-2,3-dihydro-benzo[1,4]dioxin-2(R)-yl)-methanol as an oil (1.44 g; 77%): MS (M+H)+ 307.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07368567B2
Source datasetuspto-grants-2008_05
ORD IDord-47ce150fca68458cbc16cb9fe092bc1d
Source noteuspto-grants-2008_05