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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1463364생성일: 2026년 10월 26일

1,2-Dibromoethane → 2-(3,4-Dimethoxyphenyl)-5-methoxytetrahydrofuran

https://huagongshe.com/reaction/1463364

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DibromoethaneHCID 7839—
반응물Benzene, 4-bromo-1,2-dimethoxy-HCID 76114—
반응물MagnesiumHCID 5462224—
반응물2-(Benzenesulfonyl)-5-methoxyoxolaneHCID 19930462—
촉매Zinc bromideHCID 10421208—
용매TetrahydrofuranHCID 8028—
생성물2-(3,4-Dimethoxyphenyl)-5-methoxytetrahydrofuranHCID 1993045582%

반응 단계

Magnesium (2.18 g, 0.091 M) was placed in a 3-necked flask containing dry THF (10 ml) and 1,2-dibromoethane (0.2 ml). A solution of 4-bromoveratrole (18.0 g, 0.086 M) in THF (50 ml) was added dropwise, warming to initiate reaction. The resulting solution was heated at reflux for 0.75 h then cooled to room temperature and cannulated into a 1M solution of ZnBr2 in THF (50 ml, 0.05 M) and stirred for 0.5 h at room temperature. A solution of 2-benzenesulphonyl-5-methoxytetrahydrofuran (10.0 g, 0.041 M) in THF (50 ml) was added dropwise to the pale yellow suspension and the mixture allowed to stir at room temperature for 20 h. Reaction was quenched by addition of 1N HCl (50 ml), and extracted with ether (2×100 ml). The organics were combined washed with water (50 ml) dried (Na2SO4) and evaporated. Flash column chromatography (flash silica gel, hexane:ethyl acetate (3:2)) gave 2-(3,4-dimethoxyphenyl)-5-methoxytetrahydrofuran (8.0 g, 82%) as a yellow oil (rf 0.28).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05300524
출처 데이터셋uspto-grants-1994_04
ORD IDord-3574e14ed1dd4b42aba45a1eca06b6c5
출처 메모uspto-grants-1994_04