HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 2-Ethoxycarbonylimino-3-(3-trifluoromethylpheny)-5-bromothiazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-Ethoxycarbonylimino-3-(3-trifluoromethylphenyl)thiazolidine | HCID 54225833 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-Ethoxycarbonylimino-3-(3-trifluoromethylpheny)-5-bromothiazoline | HCID 54096993 | 45.3% |
Reaction Steps
A solution of 2-ethoxycarbonylimino-3-(3-trifluoromethylphenyl)thiazolidine (1.6 g) and N-bromosuccinimide (2 g) in chloroform (50 ml) was refluxed for 10 hours. After cooling, the reaction mixture was washed with an aqueous sodium sulfite solution and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure, and the residue was subjected to column chromatography to give 0.9 g of 2-ethoxycarbonylimino-3-(3-trifluoromethylpheny)-5-bromothiazoline (Compound No. 30).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05426188 |
| Source dataset | uspto-grants-1995_06 |
| ORD ID | ord-e9219addc6ce432f8c50f7527d001711 |
| Source note | uspto-grants-1995_06 |