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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1877967생성일: 2026년 10월 26일

Diethylamine → 3-[3-(2-Bromobenzyl)-3H-imidazol-4-yl]-3-methylbutan-1-ol

https://huagongshe.com/reaction/1877967

반응식

참여 물질

역할이름HCID투입량
반응물DiethylamineHCID 8021—
반응물2-Bromobenzyl bromideHCID 76965—
반응물Sodium BicarbonateHCID 516892—
반응물1,4-Dioxane hydrochlorideHCID 20443148—
반응물4-[3-(tert-butyldimethylsilanyloxy)-1,1-dimethylpropyl]-1-trityl-1H-imidazoleHCID 53630868—
용매MethanolHCID 887—
용매AcetonitrileHCID 6342—
생성물3-[3-(2-Bromobenzyl)-3H-imidazol-4-yl]-3-methylbutan-1-olHCID 58827196—

반응 조건

온도80 °C

반응 단계

To a solution of 4-[3-(tert-butyldimethylsilanyloxy)-1,1-dimethylpropyl]-1-trityl-1H-imidazole (650 mg, 1.27 mmol) in CH3CN (10 mL) at ambient temperature is added a solution of 2-bromobenzyl bromide (420 mg, 1.68 mmol) in CH3CN (10 mL). The resulting solution is stirred at 80° C. for 6 h. The mixture is cooled to ambient temperature and diethylamine (2 mL) is added, followed by MeOH (10 mL) and the mixture is heated at 75° C. for 1 hr and stirred at ambient temperature overnight. To the reaction mixture is added HCl/dioxane (4 M, 5 mL, 20 mmol) and stirred at ambient temperature for 1 h. The mixture is neutralized with saturated aqueous NaHCO3 and concentrated. The residue is partitioned between CH2Cl2 and brine. The organic layer is washed with brine, dried over Na2SO4 and concentrated to give an oil, which is subjected to flash chromatography (silica gel) eluting with MeOH:CH2Cl2 to yield the desired compound. MS (ESI) m/z 323 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08314097B2
출처 데이터셋uspto-grants-2012_11
ORD IDord-989eb4082d89420d886d69543aab1425
출처 메모uspto-grants-2012_11