참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Phenol | HCID 996 | — |
| 반응물 | 4-Hydroxybenzoic acid hydrazide | HCID 1742 | — |
| 반응물 | Benzenamine hydrochloride (1:1) | HCID 8870 | — |
| 반응물 | Phenylparaben | HCID 87250 | — |
| 생성물 | 3,5-Bis(4-hydroxyphenyl)-4-phenyl-1,2,4-triazole | HCID 136026355 | 50% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05245043 |
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| 출처 데이터셋 | uspto-grants-1993_09 |
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| ORD ID | ord-7b40b92986b142c0b4b761dffa4e4a2f |
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| 출처 메모 | uspto-grants-1993_09 |
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