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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2233198Generated: October 31, 2026

4-Methoxybenzyl alcohol → 4-Methoxybenzyl bromide

https://huagongshe.com/reaction/2233198

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxybenzyl alcoholHCID 7738—
ReactantPhosphorus tribromideHCID 24614—
SolventDiethyl EtherHCID 3283—
Product4-Methoxybenzyl bromideHCID 165021—

Reaction Steps

A solution of 4-methoxybenzyl alcohol (6.2 ml, 50 mmol) in dry ether (120 ml) was treated dropwise with phosphorus tribromide (2.07 ml, 22 mmol). The mixture was heated under reflux for 1 hour, cooled, washed twice with water, dried and the solvent was evaporated. The 4-methoxybenzyl bromide thus produced was added to a mixture of 4-bromo-1,2-dihydro-3,6-pyridazinedione (for a synthesis, see Example 3(a) above) (4 g, 21 mmol) and potassium carbonate (8.28 g, 60 mmol) in dry DMF (60 ml) and stirred overnight at RT. The mixture was diluted with ethyl acetate, washed 3 times with water, dried over magnesium sulfate and evaporated to low volume. Some solid was filtered off and washed with ethyl acetate. The filtrate was evaporated to dryness and the residue chromatographed on silica, eluting with 20% ethyl acetate/hexane and then 100% ethyl acetate. This gave the less polar of the two desired products (3.233 g), the more polar of the two desired products (1.626 g) and a mixture of these (1.351 g). Total yield 6.30 g, 70%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709483B2
Source datasetuspto-grants-2010_05
ORD IDord-bf4bc6f8a0b94e6e96813be770933f42
Source noteuspto-grants-2010_05