Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261498Generated: November 3, 2026

2-Bromothiophene → 2-(2-Methoxyphenyl)thiophene

https://huagongshe.com/reaction/2261498

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromothiopheneHCID 13851—
ReactantAmmonium ChlorideHCID 25517—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2-Methoxyphenylboronic acidHCID 2733958—
CatalystTriphenylphosphineHCID 11776—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Solvent1,2-DimethoxyethaneHCID 8071—
Product2-(2-Methoxyphenyl)thiopheneHCID 356419095%

Reaction Steps

2-Bromothiophene (7.2 g, 43.9 mmol), 2-methoxyphenylboronic acid (6.7 g, 43.9 mmol), palladium acetate (0.14 g, 0.62 mmol), triphenylphosphine (0.6 mg, 2.3 mmol) and potassium phosphate (9.40 g, 44.3 mmol) were added to a flask. A mixture solution of 10 mL of water and 40 mL of dimethoxyethane was added and reflux was performed for 6 hours. After cooling to room temperature, aqueous ammonium chloride solution (50 mL) and diethyl ether (100 mL) were added. The organic layer was separated. After extracting the residue using diethyl ether, the collected organic layer was dried with magnesium sulfate. After removing volatile materials, followed by purification via silica gel chromatography using hexane, 7.9 g (yield: 95%) of 2-(2′-methoxyphenyl)thiophene was obtained as colorless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07847039B2
Source datasetuspto-grants-2010_12
ORD IDord-d7d2d4a2c62e43c1871b8c18f0c2da81
Source noteuspto-grants-2010_12