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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 880603Generated: November 2, 2026

Iodine → HCID 83535263, compound

https://huagongshe.com/reaction/880603

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantPyridineHCID 1049—
ReactantSodium ThiosulfateHCID 24477—
ReactantThioureaHCID 2723790—
Reactantp-FluorobenzoylacetonitrileHCID 2783172—
SolventEthanolHCID 702—
ProductHCID 83535263HCID 83535263—

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 4-fluorobenzoylacetonitrile (50 g, 306 mmol, 1 eq.) in EtOH (600 mL) was added pyridine (24.7 mL, 306 mmol, 1 eq.). The resulting mixture was stirred at 70° C. for 15 min then cooled to r.t. A previously stirred suspension of thiourea (46.7 g, 613 mmol, 2 eq.) and iodine (77.8 g, 306 mmol, 1 eq.) in EtOH (300 mL) was then slowly added. After 1 h at r.t. a cold 1 M Na2S2O3 solution (360 mL) was added under stirring. The resulting precipitate was filtered, washed with water, and finally dried under vacuo to afford 2-Amino-4-(4-fluoro-phenyl)-thiazole-5-carbonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993590B2
Source datasetuspto-grants-2015_03
ORD IDord-fd0776f05a314625929195c8ff0adb2d
Source noteuspto-grants-2015_03