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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 357704생성일: 2026년 10월 26일

Pyridine → 5-(Bromomethyl)-1,2,3-trimethoxybenzene

https://huagongshe.com/reaction/357704

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Phosphorus tribromideHCID 24614—
반응물3,4,5-Trimethoxybenzyl alcoholHCID 77449—
용매TetrahydrofuranHCID 8028—
생성물5-(Bromomethyl)-1,2,3-trimethoxybenzeneHCID 10355271202.8%

반응 조건

온도0 °C

반응 단계

To a solution of 3,4,5-trimethoxybenzyl alcohol (20.2 g, 0.108 mol) in 300 ml of dry tetrahydrofuran was added 4.12 ml (0.052 mol) of pyridine, and cooled to 0° C. A solution of phosphorous tribromide (4.8 ml, 0.051 mol) in 20 ml of dry tetrahydrofuran was added dropwise to the above solution at 0 ° C. The mixture was stirred for 1 hr. Tetrahydrofuran was concentrated. The residue was then diluted with 200 ml of 10% hydrochloric acid, and then extracted with 200 ml of ethyl acetate. The extract was dried over magnesium sulfate, filtered, concentrated, and dried in vacuum overnight. 3,4,5-Trimethoxybenzyl bromide (27 g, 100% yield) was obtained as a white solid, which can be used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05840991
출처 데이터셋uspto-grants-1998_11
ORD IDord-d81fec49ae5444638cd057f3f55b7c37
출처 메모uspto-grants-1998_11