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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 620706Generated: October 29, 2026

1-Bromooctane → 1-(Octyloxy)-4-(2,4,4-trimethylpentan-2-yl)benzene

https://huagongshe.com/reaction/620706

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromooctaneHCID 8140—
Reactant4-Tert-octylphenolHCID 8814—
ReactantPotassium CarbonateHCID 11430—
SolventDimethylformamideHCID 6228—
Product1-(Octyloxy)-4-(2,4,4-trimethylpentan-2-yl)benzeneHCID 2124400581%

Reaction Conditions

Temperature50 °C

Reaction Steps

To 700 ml of N,N-dimethylformamide were added 206 g of 4-t-octylphenol and 207 g of anhydrous potassium carbonate and the mixture was stirred at 50° C. To the mixture was added dropwise 251 g of 1-bromooctane and thereafter the mixture was stirred for 7 hours at 65° to 80° C. Then, after removing insoluble matter by filtration, water was added to the filtrate thus obtained and the product was extracted with ethyl acetate. The organic solvent layer was collected, washed with a saturated aqueous sodium chloride solution, dried on anhydrous magnesium sulfate, and concentrated under reduced pressure. The oily material thus obtained was distilled under reduced pressure (169°-172° C./0.05-0.06 mmHg) to provide 257 g (81% in yield) of 1-octyloxy-4-t-octylbenzene (Compound A).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04822730
Source datasetuspto-grants-1989_04
ORD IDord-b3baf37056c242aab44d43951e06d2e4
Source noteuspto-grants-1989_04