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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1194836Generated: October 25, 2026

Nicotinic Acid → Nicotinoyl chloride

https://huagongshe.com/reaction/1194836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNicotinic AcidHCID 938—
ReactantThionyl ChlorideHCID 24386—
Reactant4-(4-Tert-butylphenoxy)butan-1-OLHCID 13313737—
SolventDichloromethaneHCID 6344—
ProductNicotinoyl chlorideHCID 82604—

Reaction Steps

Nicotinoyl chloride was prepared by treating 100 g (0.81 mole) of nicotinic acid with 280 ml of thionyl chloride at reflux for two hours. The excess thionyl chloride was removed in vacuo and the crystalline acid chloride hydrochloride was suspended in 500 ml of dichloromethane. To the stirred mixture was added 66 g (0.30 mole) of 4-p-t-butylphenoxy-1-butanol dissolved in 400 ml of dichloromethane. After forty-eight hours the mixture was washed with one liter of saturated sodium bicarbonate. The dichloromethane solution was dried over magnesium sulfate and evaporated to a syrupy residue. The material was chromatographed on 1 kg of silica gel with elution by dichloromethanemethanol, 96:4, to afford 43.8 g (45%) of the nicotinate ester as an oil. The hydrobromide salt was prepared by treatment of a solution of 43.8 g in 800 ml of ethyl acetate with 30 ml of 4.5N hydrogen bromide in ether. The precipitate was collected, washed with pentane and dried, m.p. 132°-133° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04816491
Source datasetuspto-grants-1989_03
ORD IDord-33399a1a2d45496a9b74565a90b31edd
Source noteuspto-grants-1989_03