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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097268Generated: October 27, 2026

Nicotinic Acid → Chloromethyl nicotinate

https://huagongshe.com/reaction/1097268

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNicotinic AcidHCID 938—
Reactant(Chloromethyl)sulfonyl chlorideHCID 77054—
ReactantSodium BicarbonateHCID 516892—
ReactantBis(tetrabutylammonium) sulphateHCID 11433187—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductChloromethyl nicotinateHCID 1460883025.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of nicotinic acid (200 mg, 1.6 mmol), sodium bicarbonate (540 mg, 6.4 mmol), and tetrabutylammonium sulfate (54 mg, 0.16 mmol) was dissolved in a mixture of 4 ml of dichloromethane and 4 ml of water, and cooled to 0° C. To this stirred mixture was added chloromethylchlorosulfone (165 μl, 1.6 mmol) in 1 ml of dichloromethane, and the mixture was allowed to warm to room temperature, stirring overnight. The organic layer was separated, washed with brine, dried over sodium sulfate, and concentrated under reduced pressure to a yellow oil, which was dissolved in dichloromethane and filtered through a silica plug. Removal of the solvent under reduced pressure provided chloromethyl pyridine-3-carboxylate (70 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143249B2
Source datasetuspto-grants-2012_03
ORD IDord-8946598f922f477e912ede868215ac44
Source noteuspto-grants-2012_03