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HRID 2606생성일: 2026년 10월 24일

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/ko/reaction/2606

반응식

참여 물질

역할이름HCID투입량
반응물HexaneHCID 8058—
반응물Ethyl 4-(diethoxyphosphoryl-3,3-dimethoxypropyl)benzoateHCID 57037360—
반응물1-(Tol-4-yl)3,4-dihydro-4,4-dimethyl-7-naphthaldehydeHCID 86588677—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물Ethyl 4-[1-(2,2-dimethoxyethyl)-2-{1(tol-4-yl)3,4-dihydro-4,4-dimethyl-naphthalen-7-yl}-(E)-ethenyl]-benzoateHCID 86588679—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05728846
출처 데이터셋uspto-grants-1998_03
ORD IDord-1b0e8d298ae64c8b9df10e43febd3af1
출처 메모uspto-grants-1998_03