HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1282432Generated: November 1, 2026
4-Chlorobenzenesulfonyl chloride → HCID 18424427, compound
https://huagongshe.com/reaction/1282432
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Chlorobenzenesulfonyl chloride | HCID 7398 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-Fluoro-2-fluoromethyl-3-butyn-2-ol | HCID 18424428 | — |
| Reactant | HCID 21921625 | HCID 21921625 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18424427 | HCID 18424427 | 75% |
Reaction Steps
An amount (1.2 g) of 1-fluoro-2-fluoromethyl-3-butyn-2-ol and p-chlorobenzenesulfonyl chloride (2.1 g) were dissolved in tetrahydrofuran (10 ml); to the solution under cooling with ice, 60% oily sodium hydride (0.48 g) was added under a nitrogen atmosphere. After the end of the addition, the mixture was stirred for 4 hours while its temperature was raised to room temperature. A hexane/ethane mixed solvent (1/1) was added to the reaction mixture, which was then washed with water and a saturated aqueous solution of sodium chloride, dried with anhydrous sodium sulfate and concentrated under reduced pressure. The resulting residue was subjected to silica gel column chromatography (eluent; hexane/methylene chloride=1/1) and then recrystallized from methylene chloride/hexane to give the titled compound (2.2 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06455708B1 |
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| Source dataset | uspto-grants-2002_09 |
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| ORD ID | ord-e85547b9b0774313a6024f9ccff191b6 |
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| Source note | uspto-grants-2002_09 |
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