HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716307Generated: October 26, 2026
Bromochloromethane → 1-Chloromethanesulfonyl-4-fluoro-benzene
https://huagongshe.com/reaction/1716307
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromochloromethane | HCID 6333 | — |
| Reactant | 4-Fluorobenzenesulfonyl chloride | HCID 9588 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Chloromethanesulfonyl-4-fluoro-benzene | HCID 58904791 | — |
Reaction Steps
A stirred mixture of 4-fluoro-benzenesulfonyl chloride (10.16 g, 52.2 mmol), sodium sulfite (12.25 g, 97.1 mmol) and sodium bicarbonate (8.02 g, 95.5 mmol) in water (55 mL) is heated at 100° C. for 1 h. The crude sodium sulfinate solution is allowed to cool for 30 min and then treated with bromochloromethane (60 mL) and tetra-N-butyl ammonium bromide (1.68 g, 5.22 mmol). The resulting mixture is heated at 75° C. overnight. The organic layer was separated. The aqueous solution was extracted with CH2Cl2 (×2). The combined organics were washed with water and brine, and dried over anhydrous MgSO4. The filtration through Celite-silica gel pad and concentration in vacuo gave the desired product without further purification. 1H NMR (300 MHz, CDCl3) 8.00 (m, 2H), 7.30 (m, 2H), 4.53 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07803793B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-4f0070da010e41599cb07fe778827ad4 |
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| Source note | uspto-grants-2010_09 |
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