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HRID 446763作成日:2026年10月25日

Dimethylformamide → p-Cyclohexylbenzaldehyde

https://huagongshe.com/reaction/446763

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物1-Bromo-4-cyclohexylbenzeneHCID 90718—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物p-CyclohexylbenzaldehydeHCID 11968938%

反応条件

温度-78 °C

反応手順

To a solution of 1-bromo-4-cyclohexylbenzene (850 mg, 3.55 mmol) in THF (4.0 mL) was added n-BuLi (3.1 mL, 4.62 mmol) at −78° C. under an inert atmosphere. The reaction mixture was stirred for 60 min at −78° C., and then DMF (2.8 mL) was added. The reaction mixture was then stirred for an additional hour at −78° C., warmed to 0° C., and quenched with a saturated NH4Cl solution. The mixture was then extracted with ethyl acetate (2×30 mL). The combined organic layers were then dried over magnesium sulfate, filtered and concentrated in vacuo to obtain the crude product. The crude material was purified via silica gel column chromatography to afford 4-cyclohexylbenzaldehyde (250 mg, 38%) as a solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08481532B2
出典データセットuspto-grants-2013_07
ORD IDord-fd5d4f03234a4af58d408505126654dd
出典メモuspto-grants-2013_07