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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2109050Generated: October 25, 2026

Diisopropylamine → 4-Chloronicotinic acid hydrochloride

https://huagongshe.com/reaction/2109050

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
Reactant4-ChloropyridineHCID 12288—
ReactantSodium HydroxideHCID 14798—
ReactantAcetone cardiceHCID 18522661—
ReactantHCID 178418244HCID 178418244—
SolventCarbon DioxideHCID 280—
SolventTetrahydrofuranHCID 8028—
Product4-Chloronicotinic acid hydrochlorideHCID 67220186—

Reaction Steps

To a solution of diisopropylamine (20.0 g) in tetrahydrofuran (200 ml) is added dropwise 1.6 M n-butyllithium/n-hexane solution under ice-cooling. The mixture is then stirred for 30 minutes under the same cooling conditions. The reaction mixture is cooled with dry ice-acetone, and thereto is added dropwise a solution of 4-chloropyridine (20.4 g) in tetrahydrofuran (100 ml). The mixture is then stirred for 20 minutes under the same cooling conditions. The resulting reaction solution is poured in crushed dry ice in a portion and then warmed to room temperature. The reaction solution is cooled with ice and basified by addition of sodium hydroxide, followed by concentration under reduced pressure. The resulting residue is dissolved in water and washed with dichloromethane. The aqueous layer is cooled with ice and acidified with conc. hydrochloric acid. The precipitates are collected by filtration and dried to give 4-chloronicotinic acid hydrochloride (21.4 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514449B2
Source datasetuspto-grants-2009_04
ORD IDord-fccba68c89ba4eb3b5e2bc054a56df00
Source noteuspto-grants-2009_04