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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1283549Generated: October 29, 2026

Hydrochloric Acid → N-[2-Methylamino-2-methylpropyl]benzamide

https://huagongshe.com/reaction/1283549

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl AcetateHCID 8857—
ReactantN-[2-benzylmethylamino-2-methylpropyl]benzamideHCID 21409888—
ReactantHCID 21409933HCID 21409933—
CatalystPalladium ChlorideHCID 24290—
SolventAcetic AcidHCID 176—
SolventDiethyl EtherHCID 3283—
ProductN-[2-Methylamino-2-methylpropyl]benzamideHCID 2140981970%

Reaction Steps

N-[2-benzylmethylamino-2-methylpropyl]benzamide (3.55 g.,) was dissolved in glacial acetic acid (30 ml.) and hydrogenated over palladium chloride (140 mg.) 320 ml of H2 was taken up. The catalyst was filtered and the filtrate washed with ether (2 × 100 ml.). The filtrate was then made alkaline with 5N sodium hydroxide and extracted with ether (3 × 60 cm3). The ether extrcts were dried (anhyd. Na2SO4), filtered and the excess ether evaporated under reduced pressure to give a liquid residue (2.7 g.) the liquid was dissolved in ether (30 ml.). To this was added ethereal HCl in a dropwise manner. The excess ether was evaported under reduced pressure to give a sticky solid which was refluxed with ethyl acetate for two hours. On cooling crystals of N-[2-methylamino-2-methylpropyl]benzamide hydrochloride were obtained in 70% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03975443
Source datasetuspto-grants-1976_08
ORD IDord-15cb5a9c2cbb47ac8c3da515cac34296
Source noteuspto-grants-1976_08