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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 974501생성일: 2026년 10월 24일

4-Fluorobenzophenone → 1-(4-Fluorophenyl)-2-(1-methyl-1H-tetrazol-5-yl)-1-phenylethanol

https://huagongshe.com/ko/reaction/974501

반응식

참여 물질

역할이름HCID투입량
반응물4-FluorobenzophenoneHCID 67663—
반응물1,5-DimethyltetrazoleHCID 78825—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물1-(4-Fluorophenyl)-2-(1-methyl-1H-tetrazol-5-yl)-1-phenylethanolHCID 1472402262%

반응 조건

온도-78 °C

반응 단계

A solution of 1,5-dimethyltetrazole (29.25 g; 0.298 mole) in dry THF (400 mL) was cooled to -78° C. and treated with n-butyllithium (133 mL of a 2.5M solution in hexane; 0.3325 mole) over 30 minutes. The mixture was stirred at -78° C. for 30 minutes and treated with 4-fluorobenzophenone (50 g, 0.25 mole. The mixture was stirred at -78° C. for 30 minutes and allowed to warm up to 23° C. over 2 hours. The reaction was quenched with 2N HCl (100 mL) and the organic solvent was removed by evaporation. The residue was extracted with CHCl3 (2×100 mL) and the combined organic layers were dried (Na2SO4) and evaporated to afford a brown oil. Purification by chromatography using 20% EtOAc-hexane as eluent afforded the title compound as a white solid (46.3 g; 62%). m.p.=113°-114° C. (crystallized from EtOAc-hexane). MS (CI): m/e=299 for (M+H)+ ;

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05068346
출처 데이터셋uspto-grants-1991_11
ORD IDord-cc3cde0bbb62497c868a9e9b7f8d26aa
출처 메모uspto-grants-1991_11