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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

반응식

참여 물질

역할이름HCID투입량
반응물Trityl chlorideHCID 6456—
반응물Sodium hydrideHCID 24758—
반응물4-(3-bromophenyl)-2,4-dihydro-3H-1,2,4-triazol-3-oneHCID 67160367—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물4-(3-bromophenyl)-2-(triphenylmethyl)-2,4-dihydro-3H-1,2,4-triazol-3-oneHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822518B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-0734f608f1114eb39f45df0a454ca0aa
출처 메모uspto-grants-2014_09