돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5566생성일: 2026년 10월 23일

Phenol → 3,5-Bis(4-hydroxyphenyl)-4-phenyl-1,2,4-triazole

https://huagongshe.com/ko/reaction/5566

반응식

참여 물질

역할이름HCID투입량
반응물PhenolHCID 996—
반응물4-Hydroxybenzoic acid hydrazideHCID 1742—
반응물Benzenamine hydrochloride (1:1)HCID 8870—
반응물PhenylparabenHCID 87250—
생성물3,5-Bis(4-hydroxyphenyl)-4-phenyl-1,2,4-triazoleHCID 13602635550%

반응 조건

온도220 °C

반응 단계

Into a 500 ml three neck round bottom flask equipped with a magnetic stirbar, nitrogen inlet, glass stopper, and distillation head was placed 4-hydroxybenzoic hydrazide (60.9 g, 0.4 mol) and phenyl-4-hydroxybenzoate (85.7 g, 0.4 mol). The mixture was heated to approximately 220° C. by use of a Wood's metal bath. The solids melt and phenol began to evolve and was removed via the distillation head. After two hours, aniline hydrochloride (103.6 g, 0.8 mol) was added and the temperature was increased to 250° C. and held for two hours. The mixture was cooled and washed repeatedly in methanol to give a white solid (65.8 g, 50% yield). The solid was recrystallized from N,N-dimethylacetamide (approximately 225 ml) to give, after drying at 200° C. under vacuum, white needles (49.7 g, 37% yield) with a melting point of approximately 420° C. by differential thermal analysis (DTA). Elemental analysis for C20H15N3O2 : Calculated: C, 72.93%; H, 4.59%; N, 12.76%; O, 9.72%. Found: C, 72.97%; H, 4.63%; N, 12.84%. This monomer has the following structure: ##STR8##

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05245043
출처 데이터셋uspto-grants-1993_09
ORD IDord-7b40b92986b142c0b4b761dffa4e4a2f
출처 메모uspto-grants-1993_09