돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 218251생성일: 2026년 10월 25일

Triphenyl(3,4,5-trimethoxybenzyl)phosphonium bromide → 4-Bromo-6-[(Z)-2-(3,4,5-trimethoxyphenyl)vinyl]-1,2-di(tert-butyldimethylsilyloxy)benzene

https://huagongshe.com/reaction/218251

반응식

참여 물질

역할이름HCID투입량
반응물Triphenyl(3,4,5-trimethoxybenzyl)phosphonium bromideHCID 370917—
반응물HCID 60130680HCID 60130680—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
용매tert-Butyl methyl etherHCID 15413—
생성물4-Bromo-6-[(Z)-2-(3,4,5-trimethoxyphenyl)vinyl]-1,2-di(tert-butyldimethylsilyloxy)benzeneHCID 6013067255.9%

반응 조건

온도0 °C

반응 단계

A suspension of 3,4,5-trimethoxybenzyltriphenylphosphonium bromide (1.69 g, 3.23 mmol) in tetrahydrofuran (30 mL) was cooled to 0° C. and butyllithium (2 mL of a 1.6 N solution in hexane, 3.23 mmol) was added dropwise. The brick red solution was stirred at 0° C. for 20 min, then a solution of 19 (0.96 g, ca 2.2 mmol) in tetrahydrofuran (12 mL) was added dropwise. The temperature was allowed to rise to room temperature overnight, than the reaction was diluted with tert-butylmethyl ether (ca 100 mL) and washed with water (ca 50 mL, containing 1 mL 2N HCl) then brine (30 mL). The organic layer was dried over sodium sulphate and the solvent removed under reduced pressure to give a crude which was purified by column (elution with cyclohexane:AcOEt 10:1) to give 0.75 g of 20 still impure with 20% of the E isomer.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08198302B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-ae5a82024ead43189050401038470273
출처 메모uspto-grants-2012_06