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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 596662생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/596662

반응식

참여 물질

역할이름HCID투입량
반응물HexamethylenetetramineHCID 4101—
반응물1-[4-(Bromomethyl)phenyl]-2,2-dimethylpropan-1-oneHCID 12831007—
용매ChloroformHCID 6212—
생성물1-(4-Pivaloylbenzyl)-3,5,7-triaza-1-azonia-adamantane bromideHCID 20359395—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04011340
출처 데이터셋uspto-grants-1977_03
ORD IDord-a295846a0b72407e88e769fd76c5edec
출처 메모uspto-grants-1977_03