HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → N-(2-Phenylpropan-2-yl)glycinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | HCID 13142344 | HCID 13142344 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(2-Phenylpropan-2-yl)glycinamide | HCID 21516969 | — |
Reaction Steps
A solution of 2-chloro-N-(α,α-dimethylbenzyl)-acetamide (11.5 g; 0.054 mole) in ethanol (300 ml) was cooled to 0°C. The solution was saturated with ammonia (5 hours). Stirring was continued at room temperature for about 6 days. The solvent was removed under vacuum. The oily residue was taken up in 2N HCl and filtered. The filtrate was made alkaline by the addition of 2N NaOH. The alkaline phase was extracted three times with ether. The organic layer was dried over, anhydrous Na2SO4 and the solvent was evaporated. The N1 -(α,α-dimethylbenzyl)glycineamide was obtained as a light brown oil. Yield: 6.5 g (62.5 %).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03976771 |
| Source dataset | uspto-grants-1976_08 |
| ORD ID | ord-cab9a6b5a8b748b48da3e766d871f85a |
| Source note | uspto-grants-1976_08 |