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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2395825Generated: October 30, 2026

Hexane → N-[2-(2-methylamino-2-phenylethyl)phenyl]-2,2-dimethylpropanamide

https://huagongshe.com/reaction/2395825

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantEthenamine, 2-phenyl-HCID 155076—
Reactant2,2,2'-TrimethylpropionanilideHCID 2734005—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductN-[2-(2-methylamino-2-phenylethyl)phenyl]-2,2-dimethylpropanamideHCID 1096893778%

Reaction Steps

A stirred solution of N-[(2-methyl)phenyl]-2,2-di-methylpropanamide (95.6g, 0.5mol) in THF (500 ml, dried over 4Å molecular sieves) was cooled to 0° C. and treated with 1.6M n-butyllithium in hexane (630 ml, 1.0 mol). The addition of n-butyllithium was complete after 45 minutes. During the addition, the temperature of the mixture was maintained below 10° C. with external cooling. The resultant dianion solution was aged (about 1-2 hrs) at 0° C. until the homogeneous orange solution became a white heterogeneous slurry. The dianion was then quenched with N-benzylidenemethylamine (63.7g, 0.6 mol) and aged for 30 minutes at 15°-25° C. The reaction mixture was diluted with ether (200 ml), treated with crushed ice (200g), and. stirred for 15 minutes. The organic phase was separated, washed with saturated sodium chloride, dried over anhydrous magnesium sulfate and concentrated in vacuo. The residual oil was crystallized from hexane (400 ml) at 5° C. to give N-[2-(2-methylamino-2-phenylethyl) phenyl]-2,2-dimethylpropanamide (121.2g, 0.39 mol) in 78% yield. The product had a melting point of 85°-86° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05489681
Source datasetuspto-grants-1996_02
ORD IDord-c767fb5144da4c9c82ba00d01c468e90
Source noteuspto-grants-1996_02