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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050621Generated: October 26, 2026

Potassium Carbonate → 2-[4-(Sec-butyloxy)-phenoxymethyl]-5-bromothiophene

https://huagongshe.com/reaction/2050621

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromo-5-(chloromethyl)thiopheneHCID 10198227—
Reactant4-(1-Methyl-1-propyloxy)-phenolHCID 13882004—
SolventDimethylformamideHCID 6228—
Product2-[4-(Sec-butyloxy)-phenoxymethyl]-5-bromothiopheneHCID 1465010746.2%

Reaction Conditions

Temperature20 °C

Reaction Steps

6.64 g of 4-(sec-butyloxy)-phenol and 5.52 g of potassium carbonate are heated in 50 ml of anhydrous dimethylformamide for one hour at 70° C. Subsequently, 8.46 g of 5-bromo-2-chloromethylthiophene in 20 ml anhydrous dimethylformamide is dripped in. The mixture is stirred for 6 hours at 80° C. and overnight at room temperature (about 20° C.). It is then poured into 100 ml of ice water and extracted three times with ethyl acetate, and the organic phases are dried over magnesium sulfate. The solvent is evaporated off to give a crude product which is purified by chromatography on silica gel using n-hexane/ethyl acetate (4:1) as eluant. There is obtained 6.3 g of 2-[4-(sec-butyloxy)-phenoxymethyl]-5-bromothiophene as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05013847
Source datasetuspto-grants-1991_05
ORD IDord-965ee206233a4fb1afeca5f1d14537fb
Source noteuspto-grants-1991_05