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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006949Generated: October 26, 2026

4-Methoxybenzonitrile → HCID 22503375, compound

https://huagongshe.com/reaction/1006949

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethoxybenzonitrileHCID 70129—
Reactantn-Methyl-2-methylthiophene-3-carboxamideHCID 22503091—
ReactantHCID 178420697HCID 178420697—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22503375HCID 2250337530%

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 numberUS06790844B2
Source datasetuspto-grants-2004_09
ORD IDord-68edf2d14c8e46e693393f712a601978
Source noteuspto-grants-2004_09