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HRID 1665227作成日:2026年10月27日

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

https://huagongshe.com/reaction/1665227

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物Benzene--cyclohexane (1/1)HCID 18624872—
反応物Methyl 2-(mesitylmethyl)-1-methyl-1H-benzimidazole-7-carboxylateHCID 59202086—
反応物HCID 178506846HCID 178506846—
溶媒TetrahydrofuranHCID 8028—
生成物3-[2-(Mesitylmethyl)-1-methyl-1H-benzimidazol-7-yl]pentan-3-olHCID 2498643042%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08039500B2
出典データセットuspto-grants-2011_10
ORD IDord-e8e41aa57e314f299deb3938dbda5dc9
出典メモuspto-grants-2011_10