HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → HCID 12926725, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 5-[2,6-Dichloro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoyl chloride | HCID 12926723 | — |
| Reactant | HCID 24180951 | HCID 24180951 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 12926725 | HCID 12926725 | 95.7% |
Reaction Steps
7 g of aminoacetic acid ethyl ester chloride, 20.7 g of 2-nitro-5-(2,6-dichloro-4-trifluoromethyl-phenoxy)-benzoic acid chloride and 180 ml of acetonitrile were initially introduced into the reaction vessel. 4 g of sodium hydroxide, dissolved in 10 ml of water, were added dropwise at -10° to -5° C. The reaction mixture was then poured onto water and adjusted to pH 10 and the crystalline product was filtered off. 23 g (95% of theory) of 5-(2,6-dichoro-4-trifluoromethyl-phenoxy)-2-nitro-benzoic acid (ethoxycarbonylmethyl)-amide with a melting point of 146° C. were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04889946 |
| Source dataset | uspto-grants-1989_12 |
| ORD ID | ord-1acdb8b126534fa1bf4c80aef85d6ca3 |
| Source note | uspto-grants-1989_12 |