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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1614532Generated: October 26, 2026

Amantadine → N-(Adamantan-1-yl)prop-2-enimidic acid

https://huagongshe.com/reaction/1614532

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmantadineHCID 2130—
ReactantTriethylamineHCID 8471—
ReactantAcryloyl chlorideHCID 13140—
SolventDiethyl EtherHCID 3283—
ProductN-(Adamantan-1-yl)prop-2-enimidic acidHCID 284637—

Reaction Steps

A solution of acryloyl chloride (4.05 ml, 0.05 mole) in ethyl ether (25 ml) was added to a cold (+5° C.) solution of 1-adamantaneamine (7.65 g, 0.05 mole) and triethylamine (15.3 ml, 0.11 mole) in ethyl ether (300 ml) and the solution stirred for 72 hours at room temperature. The solvent was removed on a rotary evaporator. The residue was dissoled in ethyl acetate (100 ml), washed with 10 percent hydrochloric acid (100 ml) and water (50 ml), dried over sodium sulfate, filtered and the solvent removed in vacuo leaving an oily solid which was crystallized from methanol-ethyl acetate-hexane. The structure was confirmed by NMR.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05198435
Source datasetuspto-grants-1993_03
ORD IDord-7ad86533a3154410807414295786aac6
Source noteuspto-grants-1993_03