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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2303579Generated: October 31, 2026

Hydrochloric Acid → 3-(1-Hydroxycyclobutyl)benzenesulfonamide

https://huagongshe.com/reaction/2303579

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHydroxysulfamic acidHCID 170246—
ReactantSodium AcetateHCID 517045—
Reactant1-(3-Bromophenyl)-cyclobutanolHCID 18461571—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product3-(1-Hydroxycyclobutyl)benzenesulfonamideHCID 184617224.8%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06433009B1
Source datasetuspto-grants-2002_08
ORD IDord-d4a3509bef3b495aa0082a3b932c6cbe
Source noteuspto-grants-2002_08