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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1661553Generated: October 30, 2026

Nicotinic Acid → N-Methoxy-N-methylnicotinamide

https://huagongshe.com/reaction/1661553

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNicotinic AcidHCID 938—
ReactantTriethylamineHCID 8471—
ReactantN,O-DimethylhydroxylamineHCID 14232—
ReactantThionyl ChlorideHCID 24386—
ProductN-Methoxy-N-methylnicotinamideHCID 10558996—

Reaction Steps

A flask is charged with nicotinic acid (5.0 g, 40.6 mmol). Thionyl chloride (30.0 mL) is added and the reaction is refluxed for 1 h. It is then cooled to room temperature and concentrated in vacuo. The residue is dissolved in anhydrous dichloromethane (30 mL) and O,N-dimethyl-hydroxylamine (4.35 g, 44.0 mmol) is added, followed by addition of triethylamine (14.15 g, 100.0 mmol). The reaction mixture is stirred at room temperature for 1.5 h. It is then washed with water and the aqueous phase is extracted with dichloromethane. The combined organic layer is dried over sodium sulfate and concentrated in vacuo to afford N-methyl-N-methoxy-nicotinamide as a brown oil. MS (ESI) m/z 167.0 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030334B2
Source datasetuspto-grants-2011_10
ORD IDord-921d9660561848f1aa7153685e02f075
Source noteuspto-grants-2011_10