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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 365695Generated: October 25, 2026

Ammonia → 2,6-Dimethyl-4-(2-phenylethyl)pyridine

https://huagongshe.com/reaction/365695

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantBenzyl ChlorideHCID 7503—
Reactant2,4,6-TrimethylpyridineHCID 7953—
ReactantSodium amideHCID 24533—
ReactantAmmonium ChlorideHCID 25517—
ReactantSodiumHCID 5360545—
CatalystFerrous nitrateHCID 9815404—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product2,6-Dimethyl-4-(2-phenylethyl)pyridineHCID 12733067—

Reaction Steps

Liquid ammonia (150 ml) was introduced into a 250 ml three-necked round bottomed flask equipped with a mechanical stirrer, dropping funnel and outlet tube and immersed in a dry ice/ethanol bath. Sodium amide was generated by addition of 20 mg of iron nitrate (Fe3+) followed by metallic sodium (2.09 g, 0.09 mol). The deep blue solution was stirred for one hour and a solution of collidine (1) (10.06 g, 0.083 mol) in 20 ml of dry diethylether was introduced into the reaction by addition over a period of 15 min. The resultant yellow suspension was stirred for an additional 45 min, followed by the addition or benzylchloride (6.33 g, 0.05 mol) dissolvedin 10 ml of dry diethylether. The reaction mixture was stirred for 45 min and excess sodium amide was neutralized by addition of ammonium chloride (4.82 g, 0.09 mol) dissolved in 20 ml of H2O. Ammonia was evaporated and the residue was partitioned between water and diethylether. The collected etheral phase was dried over sodium sulfate and evaporated. The brown residual oil was fractionated, and a fraction distilling at 130° C./0.1 mmHg was colelcted.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06127529
Source datasetuspto-grants-2000_10
ORD IDord-18373e60d1af4e0fa4227e2b8c350b5d
Source noteuspto-grants-2000_10