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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2120041Generated: November 1, 2026

2,5-Dimethylphenol → HCID 23437455, compound

https://huagongshe.com/reaction/2120041

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,5-DimethylphenolHCID 7267—
Reactant1-BromohexaneHCID 8101—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 67419026HCID 67419026—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 23437455HCID 23437455—

Reaction Conditions

Temperature80 °C

Reaction Steps

In 250 g of ethanol were dissolved 250 g (2.05 mol) of 2,5-dimethylphenol (or p-xylenol), 90 g (2.25 mol) of sodium hydroxide and 371 g (2.25 mol) of n-hexyl bromide. The solution was heated for 2 hours in an oil bath at 80° C. Water, 500 g, was added to the reaction mixture, from which an oily matter was separated. Vacuum distillation of the oily matter yielded 384 g of 2,5-dimethyl-1-n-hexyloxy-benzene. Next, 129 g (0.625 mol) of 2,5-dimethyl-1-n-hexyloxybenzene was dissolved in 625 g of 1,2-dichloroethane. To the solution kept in an ice bath, 100 g (0.625 mol) of bromine was added dropwise at a temperature below 5C. At the end of dropwise addition, 500 g of water was added. The organic layer was separated therefrom and washed with 300 g of an aqueous solution of 5 wt % sodium hydrogen carbonate. The organic layer was concentrated to remove the solvent, leaving an oily matter. Vacuum distillation (boiling point 114-124° C./0.5 Torr) of the oily matter yielded 174 g of 4-bromo-2,5-dimethyl-n-hexyloxybenzene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06689530B2
Source datasetuspto-grants-2004_02
ORD IDord-74869d71993943f389136507d8d44cf3
Source noteuspto-grants-2004_02