HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Ethyl 2-[4-chloro-2-(trifluoromethyl)anilino]-2-oxoacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethoxalyl chloride | HCID 20884 | — |
| Reactant | Benzenamine, 4-chloro-2-(trifluoromethyl)- | HCID 67961 | — |
| Reactant | Triethylazanium chloride | HCID 12698378 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 2-[4-chloro-2-(trifluoromethyl)anilino]-2-oxoacetate | HCID 4550962 | — |
Reaction Steps
A mixture of 2-amino-5-chlorobenzotrifluoride (14.4 ml, 0.1 mol) and triethylamine (14.0 ml, 0.1 mol) was dissolved in dry tetrahydrofuran, THF (250 ml). To this solution was added with stirring a solution of ethoxalyl chloride in THF (50 ml). After completion of the addition (30 min.) the mixture was stirred at ambient temperature for 3 h, whereafter the precipitated triethylammonium chloride was filtered off, and the filtrate was evaporated in vacuo. This left the crude title compound (24 g) as pale crystals. M.p. 55°-58° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05075304 |
| Source dataset | uspto-grants-1991_12 |
| ORD ID | ord-40569efa74154781bbc2e040ea04ff3a |
| Source note | uspto-grants-1991_12 |