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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1690027Generated: November 2, 2026

Sodium Thiosulfate → N-(2-fluoro-3-formyl-phenyl)-4-trifluoromethyl-benzenesulfonamide

https://huagongshe.com/reaction/1690027

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantTriacetoxyperiodinaneHCID 159087—
ReactantSodium BicarbonateHCID 516892—
ReactantN-(2-fluoro-3-hydroxymethyl-phenyl)-4-trifluoromethyl-benzenesulfonamideHCID 57963251—
SolventTetrahydrofuranHCID 8028—
ProductN-(2-fluoro-3-formyl-phenyl)-4-trifluoromethyl-benzenesulfonamideHCID 5796325796%

Reaction Steps

To N-(2-fluoro-3-hydroxymethyl-phenyl)-4-trifluoromethyl-benzenesulfonamide (33, 634 mg, 1.82 mmol) in 7 mL of tetrahydrofuran, Dess-Martin periodane (847 mg, 2.00 mmol) and sodium bicarbonate (2 g) were added. The reaction was stirred at room temperature for one hour, then poured into saturated aqueous sodium thiosulfate solution and extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated under vacuum and the residue was purified by silica gel column chromatography eluting with 15% ethyl acetate in hexane. Appropriate fractions were combined and concentrated under vacuum to provide the desired compound (34, 607 mg, 96%). MS(ESI) [M−H+]−=346.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153641B2
Source datasetuspto-grants-2012_04
ORD IDord-877d82c9f2ba4adb8f1e62a25faeb942
Source noteuspto-grants-2012_04