HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Ethoxycarbonylbenzoyl chloride → HCID 10407407, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Ethoxycarbonylbenzoyl chloride | HCID 12276626 | — |
| Reactant | 6-Amino-1,4,4-trimethyl-3,4-dihydroquinolin-2(1H)-one | HCID 19760227 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 10407407 | HCID 10407407 | 65.7% |
Reaction Steps
37.2 g of 6-amino-3,4-dihydro-1,4,4-trimethyl-2(1H)-quinolinone were dissolved in 600 ml of pyridine and treated dropwise at room temperature with a solution of 43 g of 4-ethoxycarbonylbenzoyl chloride in 80 ml of tetrahydrofuran. After stirring at room temperature for 20 hours, the reaction mixture was poured on to ice-water, extracted several times with ethyl acetate, the organic phase was washed with cold 2N hydrochloric acid and water, dried and evaporated. Chromatography of the crude product (silica gel, eluent hexane/ethyl acetate 2:1, then ethyl acetate) and recrystallization from ethyl acetate/hexane, yielded 45.5 g of ethyl p-[(1,2,3,4-tetrahydro-1,4,4-trimethyl-2-oxo-6-quinolinyl)carbamoyl]-benzoate, m.p. 197°-199° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05216148 |
| Source dataset | uspto-grants-1993_06 |
| ORD ID | ord-9c96a3997ddc4e319205002aeca13d5b |
| Source note | uspto-grants-1993_06 |