HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-(2-amino-4,5-dichlorophenyl)-2-ethoxy-4-cyanobenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4,5-Dichloro-1,2-phenylenediamine | HCID 79297 | — |
| Reactant | 4-Cyano-2-ethoxybenzoyl chloride | HCID 21100743 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(2-amino-4,5-dichlorophenyl)-2-ethoxy-4-cyanobenzamide | HCID 21101176 | 104.3% |
Reaction Steps
A solution of 2-ethoxy-4-cyanobenzoyl chloride (10.9 g, 52 mmol), prepared as in Preparation 11, in dichloromethane (109 ml) was added dropwise in 5 h to a solution of 4,5-dichlorophenylendiamine (18.5 g, 104.5 mmol) and triethylamine (53 g=72.6 ml, 523 mmol) in dichloromethane (550 ml). Stirring was continued for additional 2 h. The solvent was removed under vacuum and the residue was triturated with water (100 ml), filtered and dried at 50° C. under vacuum. The solid was suspended in diethyl ether (200 ml), stirred for 1 h, filtered and dried under vacuum to give 19 g of N-(2-amino-4,5-dichlorophenyl)-2-ethoxy-4-cyanobenzamide (yield 51%), mp=195–198° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07220769B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-24cf7191820048498692652b457e64c5 |
| Source note | uspto-grants-2007_05 |