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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35902Generated: October 28, 2026

Iodine → 5-(4-carboxyphenyl)-N-phenyl-4-isothiazolin-3-one

https://huagongshe.com/reaction/35902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantDichloromethaneHCID 6344—
Reactant3-(4-carboxyphenyl)-3-mercapto-N-phenylpropenamideHCID 86748656—
SolventTriethylamineHCID 8471—
Product5-(4-carboxyphenyl)-N-phenyl-4-isothiazolin-3-oneHCID 1529463854%

Reaction Steps

A mixture of 0.30 g (1.00 mmol)3-(4-carboxyphenyl)-3-mercapto-N-phenylpropenamide and 50 mL methylene chloride was stirred at room temperature. Added was 0.25 g (1.00 mmol) iodine followed by 0.2 mL (excess) triethylamine and the mixture stirred for one hour. Solvent was evaporated and 250 mL ethyl acetate added. The mixture was washed with three 100 mL portions of water. The organic layer was dried, filtered and solvent was evaporated from the filtrate. The resulting solid was triturated in absolute ethanol and filtered to dryness to provide 0.16 g (0.54 mmol, 54%)5-(4-carboxyphenyl)-N-phenyl-4-isothiazolin-3-one as a pale, yellow powder, mp=260-261° C. NMR (d6 -DMSO/TMS): 7.08 (s, 1H), 7.39-8.07 (m, 9H), 13.30 (bs, 1H). IR (KBr): 1678, 1652. Mass spectrum (CI): M/z=298.0 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05411977
Source datasetuspto-grants-1995_05
ORD IDord-2e692f64015c498284bbff59f6a36ba1
Source noteuspto-grants-1995_05