HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium tert-butoxide → 2-Ethoxycarbonylimino-3-(3-trifluoromethylphenyl) 5-methylthiazoline
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-methylthiazoline | HCID 53803418 | 64% |
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. After removal of the solvent under reduced pressure, the concentrated residue was extracted with chlorofom (100 ml), washed with water and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure, and the residue was subjected to column chromatography to give 0.36 g of 2-ethoxycarbonylimino-3-(3-trifluoromethylphenyl)-5-methylthiazoline (Compound No. 1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05244863 |
| Source dataset | uspto-grants-1993_09 |
| ORD ID | ord-559f69803bbe4b658724c6bc142b64a7 |
| Source note | uspto-grants-1993_09 |