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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2083119Generated: October 26, 2026

Hexamethylenetetramine → 1-(4-Pivaloylbenzyl)-3,5,7-triaza-1-azonia-adamantane bromide

https://huagongshe.com/reaction/2083119

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexamethylenetetramineHCID 4101—
Reactant1-[4-(Bromomethyl)phenyl]-2,2-dimethylpropan-1-oneHCID 12831007—
SolventChloroformHCID 6212—
Product1-(4-Pivaloylbenzyl)-3,5,7-triaza-1-azonia-adamantane bromideHCID 20359395—

Reaction Steps

An ice solution of 127.5 g. (0.5 mole) of α-bromo-4-pivaloyl toluene in 600 ml. of chloroform is added dropwise to 77.0 g. (0.55 mole) of hexamethylene tetramine in 550 ml. chloroform. The resulting mixture is stirred for 2 days at room temperature and the solvent evaporated in vacuo. The residue is treated with ether and the resulting solid filtered and washed thoroughly with ether to give a white solid, 1-(4-pivaloylbenzyl)-3,5,7-triaza-1-azonia-adamantane bromide. The resulting solid is suspended in 300 ml. of 6N hydrochloric acid and steam distilled until no more formaldehyde is evolved. The distillation residue is poured onto ice and 180 ml. of 50% sodium hydroxide. The basic solution is extracted with ether and the ether is washed with water, brine and dried over anhydrous magnesium sulfate, filtered and evaporated in vacuo. The residue is dissolved in ethanol and treated with ether/hydrochloric acid to give 4-pivaloyl benzylamine hydrochloride, m.p. 222° C. to 225° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04084003
Source datasetuspto-grants-1978_04
ORD IDord-2da234ea287d49da8970e966270113b3
Source noteuspto-grants-1978_04