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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 379432Generated: October 27, 2026

Methanol → 6-chloro-N,N-diethyl-4-o-tolyl-nicotinamide

https://huagongshe.com/reaction/379432

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
Reactant6-Chloro-N,N-diethylnicotinamideHCID 587813—
ReactantHCID 178424304HCID 178424304—
SolventTetrahydrofuranHCID 8028—
Product6-chloro-N,N-diethyl-4-o-tolyl-nicotinamideHCID 1216732187.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

7.62 ml (7.62 mMol) o-Tolylmagnesium chloride solution (1M in THF) were added over 15 minutes to a solution of 0.60 g (2.54 mMol) 6-chloro-N,N-diethyl-nicotinamide in 3.0 ml THF cooled to 0° C. The reaction mixture was stirred 2 hours at room temperature, then cooled again to 0° C. and 0.41 ml methanol (10.1 mMol) were added followed by 692 mg 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (3.1 mMol). After stirring 2 hours at room temperature, the reaction mixture was concentrated under reduced pressure and 50 ml t-butyl-methylether were added at 50° C. The resulting suspension was filtered off, the filtrate was concentrated and the residue was purified by flash chromatography (eluent: ethyl acetate/n-heptane 1:1) to yield 0.67 g (86%) of 6-chloro-N,N-diethyl-4-o-tolyl-nicotinamide as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06297375B1
Source datasetuspto-grants-2001_10
ORD IDord-48fab08712d94deebfc8aa9ab8fe1b9f
Source noteuspto-grants-2001_10