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HRID 596662作成日:2026年10月27日

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

https://huagongshe.com/reaction/596662

反応式

関与物質

役割名称HCID仕込み量
反応物HexamethylenetetramineHCID 4101—
反応物1-[4-(Bromomethyl)phenyl]-2,2-dimethylpropan-1-oneHCID 12831007—
溶媒ChloroformHCID 6212—
生成物1-(4-Pivaloylbenzyl)-3,5,7-triaza-1-azonia-adamantane bromideHCID 20359395—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04011340
出典データセットuspto-grants-1977_03
ORD IDord-a295846a0b72407e88e769fd76c5edec
出典メモuspto-grants-1977_03