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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 357704Generated: October 26, 2026

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

https://huagongshe.com/reaction/357704

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPhosphorus tribromideHCID 24614—
Reactant3,4,5-Trimethoxybenzyl alcoholHCID 77449—
SolventTetrahydrofuranHCID 8028—
Product5-(Bromomethyl)-1,2,3-trimethoxybenzeneHCID 10355271202.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05840991
Source datasetuspto-grants-1998_11
ORD IDord-d81fec49ae5444638cd057f3f55b7c37
Source noteuspto-grants-1998_11