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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1665227생성일: 2026년 10월 26일

Ammonium Chloride → 3-[2-(Mesitylmethyl)-1-methyl-1H-benzimidazol-7-yl]pentan-3-ol

https://huagongshe.com/reaction/1665227

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물Benzene--cyclohexane (1/1)HCID 18624872—
반응물Methyl 2-(mesitylmethyl)-1-methyl-1H-benzimidazole-7-carboxylateHCID 59202086—
반응물HCID 178506846HCID 178506846—
용매TetrahydrofuranHCID 8028—
생성물3-[2-(Mesitylmethyl)-1-methyl-1H-benzimidazol-7-yl]pentan-3-olHCID 2498643042%

반응 단계

To a solution of methyl 2-(mesitylmethyl)-1-methyl-1H-benzimidazole-7-carboxylate (1.30 g, 4.0 mmol) in tetrahydrofuran (80 mL) was added a solution of ethyllithium in benzene/cyclohexane (90/10) (0.5 M, 32 mL, 16.1 mmol) dropwise at −78° C. The solution was warmed to room temperature over 1 hr followed by addition of saturated aqueous ammonium chloride solution (20 mL). The mixture was extracted with ethyl acetate (100 mL, three times) and the combined organic layers were washed with brine (100 mL), dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was purified by silica gel column chromatography eluting with a 15-25% ethyl acetate/n-hexane gradient mixture to give the title compound (590 mg, 1.68 mmol, 42%) as a colorless solid. The resulting solid was recrystallized from n-hexane/ethyl acetate to give the title compound (435 mg, 1.24 mmol).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08039500B2
출처 데이터셋uspto-grants-2011_10
ORD IDord-e8e41aa57e314f299deb3938dbda5dc9
출처 메모uspto-grants-2011_10