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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 1-(5-benzenesulfonyl-2-(S)-oxiranylmethoxy-phenyl)-ethanone | HCID 86601557 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | (7-benzenesulfonyl-2,3-dihydro-benzo[1,4]dioxin-2(R)-yl)-methanol | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07368567B2 |
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| Source dataset | uspto-grants-2008_05 |
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| ORD ID | ord-47ce150fca68458cbc16cb9fe092bc1d |
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| Source note | uspto-grants-2008_05 |
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