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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 20256생성일: 2026년 10월 24일

1-Bromopropane → HCID 178456449, 화합물

https://huagongshe.com/ko/reaction/20256

반응식

참여 물질

역할이름HCID투입량
반응물1-BromopropaneHCID 7840—
반응물4-Amino-1,2,4-triazoleHCID 11432—
반응물4-Amino-1,2,4-triazole acetonitrileHCID 86761137—
용매AcetonitrileHCID 6342—
생성물HCID 178456449HCID 17845644997.5%

반응 단계

10.005 g 118 mmoles of 4-amino-1,2,4-triazole was weighed out and transferred to a three necked 500 ml, round bottom flask and dissolved 200 ml of acetonitrile. The solution then was stirred vigorously with an overhead stirrer the flask equipped with a reflux condenser and placed in a hot oil bath (50° C.) and allowed to heat. In a graduated cylinder, 1-bromopropane 58.865 g, 478 mmoles, was weighed out and then was slowly added to the hot 4-amino-1,2,4-triazole/acetonitrile mixture. The reaction mixture was stirred with heating for 36 hours, being monitored by thin layer chromatography, at which time the 4-amino-1,2,4-triazole was consumed. The flask was then removed from the oil bath, cooled under nitrogen atmosphere. The reaction solution was transferred to a large round bottomed flask and the acetonitrile and excess n-propyl bromide rotary evaporated away. The resultant oil was transferred to a preweighed Schlenk flask, rinsing the large flask with three 10 ml aliquots of fresh acetonitrile. The flask was evacuated for 20 hours to yield a highly crystalline solid 23.9584 g, 115 mmoles of 1-n-propyl-4-amino-1,2,4-triazolium bromide. Melting point: 63° C.; DSC onset 145° C.,

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745635B1
출처 데이터셋uspto-grants-2010_06
ORD IDord-00b3fc69ba4e4290aafd5da0ef12f7ce
출처 메모uspto-grants-2010_06