HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 20457876, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Glycolate | HCID 12184 | — |
| Reactant | HCID 20407000 | HCID 20407000 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 20457876 | HCID 20457876 | 78.4% |
Reaction Steps
A solution of 15 g of 5-(2,6-dichloro-4-trifluoromethyl- phenoxy)-2-nitro-α-phenoxypropionyl chloride in 30 ml of toluene was added dropwise to a solution of 3.7 g of ethyl hydroxyacetate and 4 g of triethylamine in 70 ml of toluene cooled to 0° to 5° C. The reaction mixture was stirred at room temperature overnight, diluted with 300 ml of toluene, washed to neutrality, dried, filtered and evaporated. 13.5 g ethoxycarbonylmethyl 5-(2,6-dicloro-4-trifluoromethyl-phenoxy)-2nitro-α- phenoxy-propionate were initially obtained in the form of a yellowish oil which then crystallised. Melting point: 75° to 76° C. The yield of pure substance was calculated to be 70.5% of theory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04452992 |
| Source dataset | uspto-grants-1984_06 |
| ORD ID | ord-db5c4912f2b94730bcff97db22581613 |
| Source note | uspto-grants-1984_06 |