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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 38985Generated: October 25, 2026

Potassium Carbonate → [7-(Methylsulfonyl)-2,3-dihydro-1,4-benzodioxin-2-YL]methanol

https://huagongshe.com/reaction/38985

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantL-ProlineHCID 145742—
Reactant(7-Bromo-2,3-dihydrobenzo[b][1,4]dioxin-2-yl)methanolHCID 233965—
ReactantSodium methanesulfinateHCID 2733271—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethyl SulfoxideHCID 679—
Product[7-(Methylsulfonyl)-2,3-dihydro-1,4-benzodioxin-2-YL]methanolHCID 66878354182.2%

Reaction Conditions

Temperature140 °C

Reaction Steps

4 batches of a mixture of (7-bromo-2,3-dihydro-1,4-benzodioxin-2-yl)methanol (0.5 g, 2.0 mmol), sodium methanesulfinate (85%) (0.37 g, 3.1 mmol), CuI (0.039 g, 0.2 mmol), L-proline (0.047 g, 0.4 mmol) and K2CO3 (0.056 g, 0.4 mmol) in DMSO (4 ml) was heated under microwave radiation to 140° C. for 1 h in a nitrogen-flushed vial. The batches were mixed and diluted with water and HCl (1 N). The resulting solution was extracted with EtOAc. The combined organic phases were washed with brine, dried and purified on flash column chromatography (isooctane/EtOAc/MeOH) to give the title compound (0.89 g). MS m/z (rel. intensity, 70 eV) 244 (M+, bp), 213 (40), 165 (27), 134 (22), 79 (18).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524766B2
Source datasetuspto-grants-2013_09
ORD IDord-3377528d9b854baa9fa119b59dfddfc1
Source noteuspto-grants-2013_09