HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanolamine → N-[2-(2-cyanophenoxy)-ethyl]-N-(5-phenyl-3-pyridylmethyl)-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | 2-Hydroxybenzonitrile | HCID 11907 | — |
| Reactant | Phosphorus trichloride | HCID 24387 | — |
| Reactant | 3-(Chloromethyl)-5-phenylpyridine | HCID 11084925 | — |
| Reactant | N-2-chloroethyl-N-(5-phenyl-3-pyridylmethyl)-amine | HCID 15511893 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | N-[2-(2-cyanophenoxy)-ethyl]-N-(5-phenyl-3-pyridylmethyl)-amine | HCID 19079381 | — |
Reaction Steps
A solution of 1.2 g 2-hydroxy-benzonitril and 2.5 g N-2-chloroethyl-N-(5-phenyl-3-pyridylmethyl)-amine [obtainable by reaction of 2-hydroxyethylamine with 3-chloromethyl-5-phenyl-pyridine and subsequent transformation of the product to the 2-chloroethyl-compound by reaction with PCl3 ] in 200 ml of acetonitrile is stirred for 5 hours at room temperature and worked up in a conventional manner to give N-[2-(2-cyanophenoxy)-ethyl]-N-(5-phenyl-3-pyridylmethyl)-amine. Stirring with 0.5 equivalenets of oxalic acid in 100 ml ethanol gives the oxalate, m.p. 208°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05767132 |
| Source dataset | uspto-grants-1998_06 |
| ORD ID | ord-6463d9177f42491bb9619708c6e6a8a1 |
| Source note | uspto-grants-1998_06 |