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HRID 256414作成日:2026年10月27日

Diisopropylamine → Methyl 1-(2-benzyloxyphenyl)methylcyclohexan-1-carboxylate

https://huagongshe.com/reaction/256414

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylamineHCID 7912—
反応物Methyl cyclohexanecarboxylateHCID 20748—
反応物1-(Benzyloxy)-2-(chloromethyl)benzeneHCID 563507—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl 1-(2-benzyloxyphenyl)methylcyclohexan-1-carboxylateHCID 1372873370%

反応条件

温度-78 °C

反応手順

Under anhydrous conditions and a nitrogen atmoshere a solution of 8.7 g (0.086 mole) diisopropylamine in 250 ml tetrahydrofuran was cooled to -78° C. and 1.6M n-butyllithium (53.75 ml, 0.086 mole) was added dropwise over ten minutes. The mixture was stirred for 45 minutes, allowed to warm to 0° C. and 12.2 g (0.086 mole) methyl cyclohexancarboxylate was added. Stirring was continued for 45 minutes and then 20 g (0.086 mole) 2-benzyloxybenzyl chloride in 20 ml tetrahydrofuran was added dropwise. The resulting mixture was stirred at room temperature for 24 hours, quenched by addition of 150 ml 3M acetic acid and stirred at room temperature for one week. The mixture was diluted with ethyl ether, washed with sodium bicarbonate solution, brine, dried (MgSO4) and concentrated to a yellow oil, 29.3 g. This was distilled to obtain 20.23 g (70%) of viscous oil, b.p. 135°-140° C. (0.4 Torr).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04703052
出典データセットuspto-grants-1987_10
ORD IDord-dc46a167edc14bad933bc94d43fa7b1f
出典メモuspto-grants-1987_10