戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 76921作成日:2026年10月23日

Diethyl Ether → (4-Butylidene-1-phenyl-cyclohexyl)-dimethylamine

https://huagongshe.com/ja/reaction/76921

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl EtherHCID 3283—
反応物TetrahydrofuranHCID 8028—
反応物4-(Dimethylamino)-4-phenylcyclohexan-1-oneHCID 11424492—
触媒Butyltriphenylphosphonium bromideHCID 159628—
生成物(4-Butylidene-1-phenyl-cyclohexyl)-dimethylamineHCID 68632980—

反応手順

Potassium tert-butylate (2.75 g, 23.7 mmol) was provided in abs. ether (50 mL) in argon and mixed with butyl-triphenyl phosphonium bromide (9.45 g, 23.7 mmol). The batch was heated for 30 min to 40° C. 4-dimethylamino-4-phenyl cyclohexanone (5.00 g, 23.0 mmol) dissolved in abs. THF (50 mL) was then added carefully in drops (exothermic reaction). The batch was heated for 6.5 h to 50° C. and stirred overnight at room temperature. The batch was then concentrated in a vacuum until dry, taken up in dioxan (20 mL) and mixed with HCl/dioxan (5 mL). A precipitate separated out during this. This was filtered off, washed with ether (10 mL), then basified with 2N NaOH and extracted with dichloromethane (2×40 mL). The organic phase was dried over Na2SO4, filtered and concentrated in a vacuum until dry.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08835689B2
出典データセットuspto-grants-2014_09
ORD IDord-fe2b2fc9c85a469fbf94e00b697aa1df
出典メモuspto-grants-2014_09