HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → N-(n-butyl)-2-[4-(5-trifloromethyl-2-pyridyloxy)phenoxy]-propionic acid amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Butylamine | HCID 8007 | — |
| Reactant | Fluazifop-methyl | HCID 155294 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | N-(n-butyl)-2-[4-(5-trifloromethyl-2-pyridyloxy)phenoxy]-propionic acid amide | HCID 13731254 | — |
Reaction Steps
A mixture containing 17.1 g (0.05 mol) of methyl 2-[4-(5-trifluoromethyl-2-pyridyloxy)-phenoxy]-propionate and 7.3 g (0.1 mol) of n-butylamine is heated at 80°-85° C. for 6 hours while stirring, then cooled and diluted with 50 ml of benzene. The benzene solution is shaken with 5% aqueous hydrochloric acid solution and then washed with water to acid-free. After separation the organic phase is dried over anhydrous sodium sulfate and evaporated to dryness. The crude product can be recrystallized from a mixture of benzene with petroleum ether (b.p. 70° C.) The compounds Nos. 1, 6, 7 and 8 are similarly prepared from the corresponding starting materials.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05199970 |
| Source dataset | uspto-grants-1993_04 |
| ORD ID | ord-38bdc57dbfaf40bea8a3a28732993448 |
| Source note | uspto-grants-1993_04 |