Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 4451Generated: October 25, 2026

2-Methyl-1-butanol → (s)-4-(6-Methyloctyloxy)benzonitrile

https://huagongshe.com/reaction/4451

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-1-butanolHCID 8723—
ReactantPotassium CarbonateHCID 11430—
Reactant4-CyanophenolHCID 13019—
Reactant1-Bromo-6-methyloctaneHCID 13548105—
SolventDimethylformamideHCID 6228—
Product(s)-4-(6-Methyloctyloxy)benzonitrileHCID 54307675—

Reaction Steps

Add 5.75 g of 4-cyanophenol 10 g of 1 brom-6-methyl octane synthesized of available active amyl alcohol, 6.67 g of anhydrous potassium carbonate, 30 ml of N,N-dimethyl formamide into 100 ml four-mouth flask under nitrogen atmosphere, allow to react for 8 hours at 110° C. After the reaction, filter the insoluble matter, then extract ether. The organic layer is then washed with 5% NaOH, water and saturated salt water, then dried and evaporated to remove the ether. Then when the obtained oily matter is refined, 11.4 g of optical (s)-4-(6-methyloctyloxy)benzonitrile is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04725688
Source datasetuspto-grants-1988_02
ORD IDord-097ce1f06049442d8b63f92135cc032e
Source noteuspto-grants-1988_02