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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52369Generated: October 29, 2026

hydroxylamine-O-sulfonic acid → HCID 9842936, compound

https://huagongshe.com/reaction/52369

Reaction equation

Participants

RoleNameHCIDCharge
Reactanthydroxylamine-O-sulfonic acidHCID 76284—
ReactantSodium AcetateHCID 517045—
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant2-methyl-3-[1-[4-[[2-(trimethylsilyl)ethyl]sulfonyl]phenyl]-4-(trifluoromethyl)-1H-imidazol-2-yl]pyridineHCID 22997772—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 9842936HCID 984293684%

Reaction Steps

To a solution of 2-methyl-3-[1-[4-[[2(trimethylsilyl)ethyl]sulfonyl]phenyl]-4-(trifluoromethyl) -1H-imidazol-2-yl]pyridine from Step 1 (0.234 g, 0.0005 mol) in 1.5 mL of dry THF was added n-Bu4NF (1.5 mL of 1.0M THF solution, 1.5 mmol). The mixture was heated to reflux for 1 hour and cooled to room temperature. A solution of sodium acetate (0.19 g, 2.3 mmol) in 3 mL of water and hydroxylamine-O-sulfonic acid (0.28 g, 2.5 mmol) were added sequentially and the mixture was stirred for 1 hour. Water (7 mL) and ethyl acetate (7 mL) were added. The organic phase was separated and washed with sat. NaHCO3 solution, water, and brine, dried over MgSO4 and filtered. The filtrate was concentrated and the residue was purified by chromatography on silica gel (ethyl acetate/acetone, 95:5) to give 0.16 g of 4-[2-(2-methylpyridin-3-yl)-4-(trifluoromethyl)-1H-imidazol-1-yl]benzenesulfonamide as a colorless solid (84%): mp 235°-237° C. Anal. Calc'd. for C16H13F3N4O2S: C, 50.26; H, 3.43; N, 14.65; S, 8.39. Found: C, 50.06; H, 3.29; N, 14.44; S, 8.52.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05616601
Source datasetuspto-grants-1997_04
ORD IDord-e29e26d3564942fbb555951d63f06aa8
Source noteuspto-grants-1997_04