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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1675140Generated: November 1, 2026

Sodium methanesulfinate → HCID 67341497, compound

https://huagongshe.com/reaction/1675140

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium methanesulfinateHCID 2733271—
Reactant(3-Bromo-5-fluorophenyl)methanolHCID 2769402—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethyl SulfoxideHCID 679—
SolventEthyl AcetateHCID 8857—
ProductHCID 67341497HCID 6734149748.2%

Reaction Conditions

Temperature90 °C

Reaction Steps

Methanesulphinic acid sodium salt (748 mg, 7.33 mmol) was added to (3-bromo-5-fluorophenyl)methanol (501 mg, 2.44 mmol) and copper(I) iodide (0.248 mL, 7.33 mmol) in DMSO (12 mL) under nitrogen. The resulting mixture was stirred at 90° C. for 3 days. The reaction mixture was diluted with EtOAc (300 mL), then filtered. The filtrate was washed sequentially with water (200 mL) and saturated brine (2×200 mL). The organic layer was dried over Na2SO4, filtered and evaporated to afford crude product. The crude product was purified by flash silica chromatography, elution gradient 70 to 100% EtOAc in isohexane. Pure fractions were evaporated to dryness to afford [3-fluoro-5-(methylsulfonyl)phenyl]methanol (240 mg, 48.1%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003649B2
Source datasetuspto-grants-2011_08
ORD IDord-efdbf89e5d3d48bda33a352e1fa21338
Source noteuspto-grants-2011_08