HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1675140Generated: November 1, 2026
Sodium methanesulfinate → HCID 67341497, compound
https://huagongshe.com/reaction/1675140
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium methanesulfinate | HCID 2733271 | — |
| Reactant | (3-Bromo-5-fluorophenyl)methanol | HCID 2769402 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 67341497 | HCID 67341497 | 48.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08003649B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-efdbf89e5d3d48bda33a352e1fa21338 |
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| Source note | uspto-grants-2011_08 |
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