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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1377179Generated: November 3, 2026

Pyridine → 1-(Bromomethyl)-2,4-dimethoxybenzene

https://huagongshe.com/reaction/1377179

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPhosphorus tribromideHCID 24614—
Reactant2,4-Dimethoxybenzyl alcoholHCID 81750—
SolventTolueneHCID 1140—
Product1-(Bromomethyl)-2,4-dimethoxybenzeneHCID 15151907—

Reaction Conditions

Temperature4 °C

Reaction Steps

2 g (11.77 mmol) of 2,4-dimethoxybenzyl alcohol (Aldrich, Steinheim, FRG) are dissolved in 30 ml of abs. toluene, and this solution is untreated with 0.3 ml of pyridine. The clear solution is cooled down to approximately 4° C. and 1.12 ml (0.992 equivalents) of PBr3 in 6 ml of abs. toluene are added dropwise to it over the space of 30 min. After a further 45 min, the reaction solution is poured onto ice-water and the whole is extracted with ether. The organic phase is washed, in succession, with water, sat. sodium bicarbonate solution and saline (all being cold). The combined aqueous phases are reextracted with ether. The combined organic phases are dried over Na2SO4 and the ether is removed on a RE at about 30° C. The toluene solution which remains, and which contains the title compound, is immediately subjected to further use. TLC (hexane:ethyl acetate, 1:1): decomposition.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05663200
Source datasetuspto-grants-1997_09
ORD IDord-fd224300a82348cfacc5af51b0c232e8
Source noteuspto-grants-1997_09