HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium tert-butoxide → 2-Ethoxycarbonylimino-3-(3-trifluoromethylphenyl)-5-methylenethiazolidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | 2-Ethoxycarbonylimino-3-(3-trifluoromethylphenyl)-5-bromomethylthiazolidine | HCID 53634945 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 2-Ethoxycarbonylimino-3-(3-trifluoromethylphenyl)-5-methylenethiazolidine | HCID 54038464 | 44.5% |
Reaction Steps
A solution of 2-ethoxycarbonylimino-3-(3-trifluoromethylphenyl)-5-bromomethylthiazolidine (0.7 g) and potassium t-butoxide (0.25 g) in t-butanol (30 ml) was refluxed for 5 hours, and the solvent was distilled off under reduced pressure. The residue was extracted with chloroform (100 ml), washed with water and dried over anhydrous magnesium sulfate. After removal of the solvent, the residue was subjected to column chromatography to give 0.25 g of 2-ethoxycarbonylimino-3-(3-trifluoromethylphenyl)-5-methylenethiazolidine (Compound (i)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05244863 |
| Source dataset | uspto-grants-1993_09 |
| ORD ID | ord-8157a175e15e4fbc96068d0c346be2c4 |
| Source note | uspto-grants-1993_09 |