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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1283944Generated: October 31, 2026

Ammonia → N-(2-Phenylpropan-2-yl)glycinamide

https://huagongshe.com/reaction/1283944

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantHCID 13142344HCID 13142344—
SolventEthanolHCID 702—
ProductN-(2-Phenylpropan-2-yl)glycinamideHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03976771
Source datasetuspto-grants-1976_08
ORD IDord-cab9a6b5a8b748b48da3e766d871f85a
Source noteuspto-grants-1976_08