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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 404834Generated: October 30, 2026

Sodium Thiosulfate → 5-Benzyl-2-(2,5-difluorophenyl)thiazole-4-carbaldehyde

https://huagongshe.com/reaction/404834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantTriacetoxyperiodinaneHCID 159087—
ReactantSodium BicarbonateHCID 516892—
Reactant(5-Benzyl-2-(2,5-difluorophenyl)thiazol-4-yl)methanolHCID 67450892—
SolventDichloromethaneHCID 6344—
Product5-Benzyl-2-(2,5-difluorophenyl)thiazole-4-carbaldehydeHCID 8669388780.1%

Reaction Steps

To a solution of (5-benzyl-2-(2,5-difluorophenyl)thiazol-4-yl)methanol (6.66 g, 20.99 mmol) in dichloromethane (70.0 mL) was added Dess-Martin periodinane (13.35 g, 31.5 mmol). The reaction mixture was stirred at room temperature for overnight. 200 mL of saturated NaHCO3 solution and saturated Na2S2O3 solution (8:1) was added for quenching the reaction. After stirred for 1 h, the reaction mixture was extracted by EtOAc. The organic layers was washed with water and brine, dried over anhydrous Na2SO4, filtered, and concentrated. The crude product was purified by column chromatography to yield 5-benzyl-2-(2,5-difluorophenyl)thiazole-4-carbaldehyde (5.3 g, 80%) as white solid. 1H NMR (CDCl3, 400 MHz): δ 10.3 (1H, s), 8.01 (1H, m), 7.36-7.17 (5H, m), 7.16-7.07 (2H, m), 4.64 (2H, s). LC/MS (uplc): MH+ 316.2, 1.21 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748626B2
Source datasetuspto-grants-2014_06
ORD IDord-d5fdff71d23a47519c6e7386ba8caa1b
Source noteuspto-grants-2014_06