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HRID 22488생성일: 2026년 10월 26일

Hexane → 2-Methoxy-5-(3,4,5-trimethoxyphenyl)oxolane

https://huagongshe.com/reaction/22488

반응식

참여 물질

역할이름HCID투입량
반응물HexaneHCID 8058—
반응물5-Bromo-1,2,3-trimethoxybenzeneHCID 75885—
반응물Magnesium BromideHCID 82241—
반응물2-(Benzenesulfonyl)-5-methoxyoxolaneHCID 19930462—
반응물ButyllithiumHCID 178418339—
촉매Zinc bromideHCID 10421208—
용매TetrahydrofuranHCID 8028—
생성물2-Methoxy-5-(3,4,5-trimethoxyphenyl)oxolaneHCID 1993045927.3%

반응 단계

To stirred solution of 1-bromo-3,4,5-trimethoxybenzene (2.47 g, 10 mmol) in THF (20 ml) at -78° C. was added 2.5M n-butyllithium in hexane (4.4 ml, 11 mmol). After 0.75 h the solution was cannulated into a mixture of 1M zinc(II) bromide in THF (11 ml, 11 mmol) and magnesium(II) bromide etherate (2.86 g, 15 mmol) in THF (10 ml) at -78° C. The resulting mixture was allowed to warm to room temperature over 1 h and then sonicated for 0.4 h. A solution of 2-benzenesulphonyl-5-methoxytetrahydrofuran (1.85 g, 7.5 mmol) in THF (10 ml)was added and the mixture stirred at room temperature for 1 h, sonicated for 1 h and stirred overnight. The reaction was quenched by the addition of aqueous ammonium chloride (20 ml). Work up and purification as described for Example 1(b) gave 2-(3,4,5-trimethoxyphenyl)-5 -methoxytetrahydrofuran (0.55 g, 27%) as a colourless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05428168
출처 데이터셋uspto-grants-1995_06
ORD IDord-ab76418b248b473985be7ed447798f4b
출처 메모uspto-grants-1995_06