HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 265730Generated: October 26, 2026
O-Xylene → 2-Imino-3-(3-trifluoromethylphenyl)-5-methylenethiazolidine
https://huagongshe.com/reaction/265730
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | O-Xylene | HCID 7237 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | N-(3-(trifluoromethyl)phenyl)-N-(2-chloro-2-propenyl)thiourea | HCID 11130193 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Imino-3-(3-trifluoromethylphenyl)-5-methylenethiazolidine | HCID 15239676 | 74.5% |
Reaction Steps
N-(3-(trifluoromethyl)phenyl)-N-(2-chloro-2-propenyl)thiourea (2.94 g) and zinc chloride (6.08 g) were added to xylene (50 ml) at room temperature, and the mixture was heated to 90° C. and stirred at the same temperature for 1.5 hour. After cooling, water was added to the reaction mixture, which was neutralized by addition of potassium hydrogen carbonate and extracted with ethyl acetate. The organic layer was washed with water. The solvent was removed by distillation under reduced pressure, and the residual oil was subjected to preparative liquid chromatography, which afforded 1.92 g of 2-imino-3-(3-(trifluoromethyl)phenyl)-5-methylidenethiazolidine (74% yield). From the results of analysis by liquid chromatography, the purity was determined to be not lower than 99%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05648533 |
|---|
| Source dataset | uspto-grants-1997_07 |
|---|
| ORD ID | ord-ccf45034ebc443e587a27e603b0e9cd1 |
|---|
| Source note | uspto-grants-1997_07 |
|---|