HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1676200Generated: October 30, 2026
Methanesulfinic acid → 4-Bromo-1-(methanesulfonyl)-2-methylbenzene
https://huagongshe.com/reaction/1676200
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanesulfinic acid | HCID 87251 | — |
| Reactant | 5-Bromo-2-iodotoluene | HCID 2724601 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 4-Bromo-1-(methanesulfonyl)-2-methylbenzene | HCID 20616765 | — |
Reaction Steps
A mixture of 4-bromo-1-iodo-2-methylbenzene (240 μL, 1.68 mmol, Aldrich), Copper(I) iodide (353 mg, 1.85 mmol, Alfa Aesar), Methanesulfinic acid, sodium salt (688 mg, 6.74 mmol, Alfa Aesar) and DMSO (7.2 mL) was purged with Argon and then heated under microwave condition at 125° C. for 20 min. The resulting mixture was stirred at 100° C. for 3 h and then cooled to room temperature. The reaction mixture was diluted with H2O and extracted with EtOAc (2×). The organic layers were combined and washed with brine, dried over Na2SO4 and concentrated in vacuo to a white solid. The solid was purified by flash chromatography (SiO2, 0-50% EtOAc in hexanes) to yield 270 mg of desired product as a white solid. MS (ESI) 249 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08003796B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-9216477e97a04b4cb160f648e08df23c |
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| Source note | uspto-grants-2011_08 |
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