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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814504Generated: November 1, 2026

4-Methoxybenzonitrile → 2-Methylthiophene-3-carboxylic acid

https://huagongshe.com/reaction/1814504

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethoxybenzonitrileHCID 70129—
Reactantn-Methyl-2-methylthiophene-3-carboxamideHCID 22503091—
ReactantHCID 178420697HCID 178420697—
SolventTetrahydrofuranHCID 8028—
Product2-Methylthiophene-3-carboxylic acidHCID 462540930%

Reaction Conditions

Temperature-70 °C

Reaction Steps

To a solution of N-methyl-2-methylthiophene-3-carboxamide (36.0 g) in THF (500 ml) was added dropwise 2.5M n-BuLi/THF solution (200 ml) at −70° C. The reaction solution was stirred at −70° C. for 2 hr. followed by the addition of anisonitrile (31.0 g) at once. After the dry ice/acetone bath was removed, the reaction mixture was back to room temperature. Three hours later, an aqueous solution of saturated ammonium chloride and ether were added thereto, and then the mixture was further stirred for 1 hr. The resulting white precipitates were collected by filtration, washed with water, ether and n-hexane in this order, and then dried, to give the title compound (17.9 g, yield; 30%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06875761B2
Source datasetuspto-grants-2005_04
ORD IDord-7bf24ba0fab24010b7cc10e1928deda1
Source noteuspto-grants-2005_04