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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1735986Generated: October 31, 2026

Sulfur Dioxide → 3-(2,5,5-Trimethyl-1,3-dioxan-2-yl)thiophene-2-sulfonamide

https://huagongshe.com/reaction/1735986

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfur DioxideHCID 1119—
Reactanthydroxylamine-O-sulfonic acidHCID 76284—
ReactantHCID 22902024HCID 22902024—
ReactantSodium Acetate TrihydrateHCID 23665404—
ReactantButyllithiumHCID 178418339—
CatalystHexaneHCID 8058—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product3-(2,5,5-Trimethyl-1,3-dioxan-2-yl)thiophene-2-sulfonamideHCID 22901938—

Reaction Steps

To a solution of 3-(2,5,5-trimethyl-1,3-dioxan-2-yl)thiophene (106 g, 0.5 mol) in hexane (1200 mL) at -60° C. was added a 2.5M solution of n-butyllithium in hexane (240 mL, 0.6 mmol) over 40 min. The mixture was allowed to warm to room temperature (approximately 1.5 hr) and then once again cooled to -60° C. and anhydrous THF (400 mL) added. Sulfur dioxide was passed over the surface of the reaction mixture for 30 min at which point the reaction mixture was allowed to warm to room temperature under a positive SO2 pressure (approximately 1 hr). The solvent was removed and the residue dissolved in water (1200 mL) to which sodium acetate trihydrate (217.73 g, 1.6 mol) was added. The solution was cooled (ice bath) to 0° C. and hydroxylamine-O-sulfonic acid (107 g, 0.95 mol) was slowly added. The mixture was stirred at room temperature for 18 hr and then extracted with ethyl acetate. The combined extracts were washed with a saturated aqueous sodium bicarbonate solution, brine, dried (Na2SO4) and evaporated to give a viscous brown oil (174.05 g); this product was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05538966
Source datasetuspto-grants-1996_07
ORD IDord-987f0326a8544d36a1cc6fd9e8d729d2
Source noteuspto-grants-1996_07