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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1061047Generated: November 3, 2026

Dimethylformamide → 6-Chloro-N-methoxy-N-methylnicotinamide

https://huagongshe.com/reaction/1061047

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantOxalyl chlorideHCID 65578—
Reactant6-Chloronicotinic acidHCID 79222—
SolventDichloromethaneHCID 6344—
Product6-Chloro-N-methoxy-N-methylnicotinamideHCID 11435597—

Reaction Steps

Under ice cooling, 6-chloronicotinic acid (5.00 g) was suspended in dichloromethane (150 ml), followed by the addition of a catalytic amount of N,N-dimethylformamide and oxalyl chloride (5.30 ml). The resulting mixture was stirred at room temperature for 23 hours. The residue obtained by concentrating the reaction mixture was dissolved in dichloromethane (100 ml), followed by the addition of N,O-dimethylhydroxylamine hydrochloride (6.18 g) and triethylamine (13.3 ml) under ice cooling. After stirring at room temperature for 6 hours, the reaction mixture was diluted with dichloromethane (150 ml), washed with a saturated aqueous solution of sodium bicarbonate, water and saturated saline and then dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent under reduced pressure was purified by chromatography on a silica gel column (hexane:ethyl acetate=2:1), whereby the title compound (6.08 g, 96%) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06525042B1
Source datasetuspto-grants-2003_02
ORD IDord-d3a4c69c5c3540d982b96e5861c339a0
Source noteuspto-grants-2003_02