Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2177349Generated: October 31, 2026

Isopropanol → HCID 22754844, compound

https://huagongshe.com/reaction/2177349

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
ReactantPotassium CarbonateHCID 11430—
ReactantBoronic acid, (4-ethylphenyl)-HCID 2734352—
Reactant2-Bromo-3-thiophenecarboxylic acidHCID 12320971—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
ProductHCID 22754844HCID 22754844—

Reaction Conditions

Temperature80 °C

Reaction Steps

Into a 50-mL sealed tube (1 atm) purged and maintained with an inert atmosphere of nitrogen, was placed 2-bromo-3-thiophenecarboxylic acid (3 g, 14.1 mmol), (4-ethylphenyl)boronic acid (2.28 g, 15.2 mmol), K2CO3 aqueous solution (35 mL, 2M, 70.2 mmol), Pd(PPh3)4 (496 mg, 0.429 mmol), IPA (30 mL) and toluene (30 mL). The resulting solution was stirred overnight at 80° C. in an oil bath. The reaction progress was monitored by TLC/LCMS (ethyl acetate/petroleum ether=1:6). The solids were filtered out and washed by 20 mL ethyl acetate. Collected the organic phases and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1:10). This resulted in 2.33 g (71%) of 2-(4-ethylphenyl)thiophene-3-carboxylic acid as light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067898B1
Source datasetuspto-grants-2015_06
ORD IDord-340f422cb37b4facb8616d52d2e0d95e
Source noteuspto-grants-2015_06