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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodine | HCID 807 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 3-(4-carboxyphenyl)-3-mercapto-N-phenylpropenamide | HCID 86748656 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 5-(4-carboxyphenyl)-N-phenyl-4-isothiazolin-3-one | HCID 15294638 | 54% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05411977 |
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| Source dataset | uspto-grants-1995_05 |
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| ORD ID | ord-2e692f64015c498284bbff59f6a36ba1 |
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| Source note | uspto-grants-1995_05 |
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