HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 10450766, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Nitro-3-(trifluoromethyl)aniline | HCID 94955 | — |
| Reactant | 2-Ethoxybenzoyl chloride | HCID 3016397 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 10450766 | HCID 10450766 | — |
Reaction Steps
2-ethoxy--benzoyl chloride was condensed with 5-Amino-2-nitrobenzotrifluoride in dichloromethane in presence of triethylamine as acid scavenger to yield 2-Ethoxy-N-(4-nitro-3-trifluromethyl-phenyl)-benzamide. The reaction mixture was then concentrated in vacuo and the residue was extracted into ethyl acetate. The ethyl acetate layer was washed with water and with cold aqueous hydrochloric acid, then dried over sodium sulphate and finally concentrated in vacuo. The residue obtained was chromatographed over silica gel to afford the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07332629B2 |
| Source dataset | uspto-grants-2008_02 |
| ORD ID | ord-eb345e951eab4874b4da5d0acbdea034 |
| Source note | uspto-grants-2008_02 |