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HRID 2606作成日:2026年10月26日

Hexane → Ethyl 4-[1-(2,2-dimethoxyethyl)-2-{1(tol-4-yl)3,4-dihydro-4,4-dimethyl-naphthalen-7-yl}-(E)-ethenyl]-benzoate

https://huagongshe.com/reaction/2606

反応式

関与物質

役割名称HCID仕込み量
反応物HexaneHCID 8058—
反応物Ethyl 4-(diethoxyphosphoryl-3,3-dimethoxypropyl)benzoateHCID 57037360—
反応物1-(Tol-4-yl)3,4-dihydro-4,4-dimethyl-7-naphthaldehydeHCID 86588677—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物Ethyl 4-[1-(2,2-dimethoxyethyl)-2-{1(tol-4-yl)3,4-dihydro-4,4-dimethyl-naphthalen-7-yl}-(E)-ethenyl]-benzoateHCID 86588679—

反応手順

To a cold (-78° C.) solution of ethyl 4-(diethoxyphosphoryl-3,3-dimethoxypropyl)benzoate (Compound D, 350 mg, 0.9 mmol, available in accordance with EPO Application No. 0 210 929 published on Feb. 4, 1987), in THF (9 mL), was added n-BuLi in hexane (1.6M solution, 0.7 mL, 1.1 mmol). The mixture was stirred for 1.5 hours. To this solution 1-(tol-4-yl)3,4-dihydro-4,4-dimethyl-7-naphthaldehyde (Compound C, 200 mg, 0.72 mmol), in THF (1 mL) was added and the mixture was gradually warmed to ambient temperature (4 h). The reaction was quenched by adding water (5 mL), and extracted with ethyl acetate (3×25 mL). The organic layer was washed with brine (10 mL), dried with MgSO4 and the solvent was removed by distillation. The crude material was purified by silicagel chromatography to afford the title compound as a colorless off.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05728846
出典データセットuspto-grants-1998_03
ORD IDord-1b0e8d298ae64c8b9df10e43febd3af1
出典メモuspto-grants-1998_03