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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1758472Generated: October 27, 2026

Hydrochloric Acid → N-methyl-2-amino-alpha-phenylphenethylamine dihydrochloride

https://huagongshe.com/reaction/1758472

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTolueneHCID 1140—
ReactantN-[2-(2-methylamino-2-phenylethyl)phenyl]-2,2-dimethylpropanamideHCID 10968937—
ProductN-methyl-2-amino-alpha-phenylphenethylamine dihydrochlorideHCID 1291516393%

Reaction Conditions

Temperature100 °C

Reaction Steps

N-[2-(2-methylamino-2-phenylethyl)phenyl]-2,2-dimethyl-propanamide (155 g, 0.5 mol) was dissolved in 6 N HCl (310 g) and stirred under a nitrogen atmosphere at 100° C. for 28 hours. The reaction mixture was cooled to 23° C. and toluene (200 ml) was added. Stirring was continued until the product had crystallized from the aqueous phase. The product was collected by filtration, washed with toluene (2×50 ml) and dried in vacuo (30 mm) at 60° C. for 60 hours to give N-methyl-2-amino-α-phenylphenethylamine dihydrochloride (139 g, 93% yield). The melting point of the product was 252°-254° C. The organic phase of the filtrate was concentrated in vacuo to give a 58% recovery of trimethylacetic acid. The aqueous phase of the filtrate afforded a second crop of N-methyl-2-amino-α-phenylphenethylamine dihydrochloride (9.3 g, 6%). The total yield of product was 99%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04374067
Source datasetuspto-grants-1983_02
ORD IDord-8e7ab7a8a0c7448687d87efb2cccd38e
Source noteuspto-grants-1983_02