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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007155Generated: October 29, 2026

Methanol → 4-(2-THIENYL)BENZYLAMINE

https://huagongshe.com/reaction/1007155

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant4-(2-thienyl)benzonitrileHCID 3564193—
ReactantAluminium lithium hydrideHCID 21226445—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product4-(2-THIENYL)BENZYLAMINEHCID 277633289%

Reaction Steps

The 4-(2-thienyl)benzonitrile (0.086 g, 0.464 mmol) was dissolved in dry tetrahydrofuran (1.6 ml) before lithium aluminum hydride (0.46 ml, 0.464 mmol, 1 M in THF) was added dropwise. The reaction was allowed to stir at room temperature overnight. TLC (5% methanol in dichloromethane) still showed starting material remaining. Another 1 eq of LAH was added. After an additional hour, the reaction was quenched by the Fieser and Fieser method using wager (17.46 μl), aqueous sodium hydroxide solution (17.46 μl, 15% soln.), and water (52.37 μl) added sequentially to the reaction. The reaction was then diluted with diethyl ether and water and extracted twice with diethyl ether before drying over sodium sulfate and concentrating in vacuo. The residue was carried on crude without any further purification. Yield=89%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06794390B2
Source datasetuspto-grants-2004_09
ORD IDord-168e996253d247ee803d963876708fb8
Source noteuspto-grants-2004_09