HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2303579Generated: October 31, 2026
Hydrochloric Acid → 3-(1-Hydroxycyclobutyl)benzenesulfonamide
https://huagongshe.com/reaction/2303579
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Hydroxysulfamic acid | HCID 170246 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 1-(3-Bromophenyl)-cyclobutanol | HCID 18461571 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 3-(1-Hydroxycyclobutyl)benzenesulfonamide | HCID 18461722 | 4.8% |
Reaction Steps
A 1.6M solution of n-butyllithium (8 ml, 12.8 mmol) in hexane was added to a solution of 1-(3-bromo-phenyl)cyclobutanol (1.44 grams, 6.4 mmol) in tetrahydrofuran at −78° C. After 30 minutes, at the reaction was allowed to warm to 0° C. Sulfur dioxide was bubbled into the reaction mixture and stirred for an additional 30 minutes. The tetrahydrofuran was evaporated and an aqueous solution of sodium acetate (4.1 grams, 50 mmol) and of hydroxylamine-sulfonic acid (1.85 grams, 16 mmol) was added. After stirring at room temperature for 2 hours, the reaction was acidified with 2N hydrochloric acid then extracted with ethyl acetate. The ethyl acetate was dried over sodium sulfate and evaporated. The residue was purified on silica gel with dichloromethane/ether to give 70 mg of the titled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06433009B1 |
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| Source dataset | uspto-grants-2002_08 |
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| ORD ID | ord-d4a3509bef3b495aa0082a3b932c6cbe |
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| Source note | uspto-grants-2002_08 |
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