HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-[4-(5-chloro-3-fluoropyridin-2-yloxy)phenoxy]propionic acid N-n-butyl-N-cyanamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Butylcyanamide | HCID 12295218 | — |
| Reactant | 2-[4-(5-Chloro-3-fluoropyridin-2-yloxy)phenoxy]propionyl chloride | HCID 19792672 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-[4-(5-chloro-3-fluoropyridin-2-yloxy)phenoxy]propionic acid N-n-butyl-N-cyanamide | HCID 88621057 | — |
Reaction Steps
While cooling with ice, a solution of 9.9 g (0.030 mole) of 2-[4-(5-chloro-3-fluoropyridin-2-yloxy)phenoxy]propionyl chloride in 30 ml of toluene is added dropwise to a solution of 3.5 g (0.035 mole) of triethylamine and 3.2 g (0.033 mole) of n-butylcyanamine in 40 m of toluene. After 5 hours, the precipitate is removed by filtration and the filtrate is purified by chromatography through silica gel. The eluate is concentrated by evaporation, affording 2-[4-(5-chloro-3-fluoropyridin-2-yloxy)phenoxy]propionic acid N-n-butyl-N-cyanamide as a yellowish oil. nD25 : 1.5482.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04640703 |
| Source dataset | uspto-grants-1987_02 |
| ORD ID | ord-a349aa3bc68045b3bab8c78b31825d81 |
| Source note | uspto-grants-1987_02 |