HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1647897Generated: October 31, 2026
Phosphorus oxychloride → HCID 19921455, compound
https://huagongshe.com/reaction/1647897
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 4-Cyanobenzoyl chloride | HCID 80172 | — |
| Reactant | HCID 15225626 | HCID 15225626 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 19921455 | HCID 19921455 | — |
Reaction Steps
4.7 g of 3-amino-4-methylamino-benzoic acid-[N-(2-methoxycarbonyl-ethyl)-amide] are first stirred at ambient temperature with 40 ml of phosphorusoxychloride, then 3.1 g of 4-cyano-benzoylchloride are added and the mixture is heated to 90° C. for 8 hours. The phosphorusoxychloride is distilled off in vacuo, the residue is stirred into 500 ml of water at 30° C. and neutralised by the addition of sodium bicarbonate in batches. The precipitate is suction filtered and extracted with ethyl acetate. The ethyl acetate phases are evaporated down, the residue is combined with the precipitate and purified by chromatography on silica gel (eluant:ethyl acetate/ethanol=100:1 to 100:5). The product obtained is decocted with ethyl acetate for final purification. Yield: 1,86 g (27% of theory), Rf value: 0.51 (silica gel; ethyl acetate/ethanol=9:1)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05434150 |
|---|
| Source dataset | uspto-grants-1995_07 |
|---|
| ORD ID | ord-8b67c3c662884c7497ee85ea4ab992cf |
|---|
| Source note | uspto-grants-1995_07 |
|---|