HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylamine → N-Ethyl-2-isobutyl-2,4-dimethylvaleramide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylamine | HCID 6341 | — |
| Reactant | 1-Bromo-2-methylpropane | HCID 6555 | — |
| Reactant | Propionitrile | HCID 7854 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 266760 | HCID 266760 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N-Ethyl-2-isobutyl-2,4-dimethylvaleramide | HCID 3016606 | — |
| Product | HCID 20565978 | HCID 20565978 | — |
Reaction Steps
2-isobutyl-2,4-dimethylpentanoyl chloride (bp. 97°-100°/16 mm) was prepared in the usual way from 2-isobutyl-2,4-dimethylpentanoic acid (prepared by the alkylation of ethyl cyanide with 2 equivalents of isobutyl bromide, followed by hydrolysis) and thionyl chloride. A solution of the acid chloride (1.5 g) in ether (20 ml) was added with stirring to a solution of ethylamine (5 ml of a 70% solution in water) in ether (100 ml). After stirring for 2 hours the ethereal layer was washed with dilute hydrochloric acid and water. The dried (MgSO4) other solution was concentrated and the residue was recrystallised from petroleum ether (bp. 40°-60°) to give N-ethyl-2-isobutyl-2,4-dimethylpentanamide, mp. 71.5°-72.5°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04296255 |
| Source dataset | uspto-grants-1981_10 |
| ORD ID | ord-358ed31041d84126ae66badeb2d50c70 |
| Source note | uspto-grants-1981_10 |