Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 70298생성일: 2026년 10월 25일
Trityl chloride → 4-(3-bromophenyl)-2-(triphenylmethyl)-2,4-dihydro-3H-1,2,4-triazol-3-one
https://huagongshe.com/reaction/70298
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Trityl chloride | HCID 6456 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 4-(3-bromophenyl)-2,4-dihydro-3H-1,2,4-triazol-3-one | HCID 67160367 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 4-(3-bromophenyl)-2-(triphenylmethyl)-2,4-dihydro-3H-1,2,4-triazol-3-one | HCID 58276623 | — |
반응 단계
A mixture of 4-(3-bromophenyl)-2,4-dihydro-3H-1,2,4-triazol-3-one (250 mg, 1.04 mmol) and NaH (50 mg of a 60% dispersion in mineral oil, 1.25 mmol) in DMF (3 mL) was stirred at room temperature for 30 min. To the solution was added 1,1′,1″-(chloromethanetriyl)tribenzene (305 mg, 1.09 mmol) and the mixture stirred at room temperature for 4 hr. The reaction mixture was diluted with EtOAc, washed with H2O and brine, dried over Na2SO4 then concentrated in vacu. The residue was purified by silica gel chromatography (EtOAc/Hexanes) to give 4-(3-bromophenyl)-2-(triphenylmethyl)-2,4-dihydro-3H-1,2,4-triazol-3-one as a pale yellow foam. 1H NMR (400 MHz, DMSO-d6) δ 7.22-7.31 (m, 15 H), 7.40-7.42 (m, 1H), 7.51 (d, J=7.8 Hz, 1H), 7.63 (d, J=7.8 Hz, 1H), 7.90 (s, 1H), 8.60 (s, 1H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08822518B2 |
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| 출처 데이터셋 | uspto-grants-2014_09 |
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| ORD ID | ord-0734f608f1114eb39f45df0a454ca0aa |
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| 출처 메모 | uspto-grants-2014_09 |
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