HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006719Generated: October 31, 2026
4-Fluorobenzenesulfonyl chloride → Sodium 4-fluorobenzene sulfinate
https://huagongshe.com/reaction/1006719
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Fluorobenzenesulfonyl chloride | HCID 9588 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Sodium 4-fluorobenzene sulfinate | HCID 421250 | — |
Reaction Steps
A solution of 4-fluorobenzenesulfonyl chloride (2 g, 10.28 mmol) in 50 mL of THF (distilled from Na-benzophenone) is cooled to 0° C. and sodium borohydride (1.9 g, 51.4 mmol) is added portionwise. The reaction is stirred at 0° C. for 2 h, then warmed to RT, and after 2 h, quenched with water (5 mL). The solvent is evaporated and the aqueous residue is acidified by addition of aqueous 6N HCl. The product is taken up in EtOAc, washed with brine, dried over anhydrous Na2SO4 and concentrated to give 4-fluorobenzenesulfinic acid: NMR (DMSO-d6) 7.12 (app t, 2H, J=8.3), 7.5 (dd, 2H, J=8.3, 6); ESI-MS 159 [M-1]−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06790978B2 |
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| Source dataset | uspto-grants-2004_09 |
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| ORD ID | ord-ad20ef8cd63848ac9f213257112838ae |
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| Source note | uspto-grants-2004_09 |
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