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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone | HCID 6775 | — |
| Reactant | 6-Chloro-N,N-diethylnicotinamide | HCID 587813 | — |
| Reactant | HCID 178424304 | HCID 178424304 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-chloro-N,N-diethyl-4-o-tolyl-nicotinamide | HCID 12167321 | 87.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06297375B1 |
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| Source dataset | uspto-grants-2001_10 |
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| ORD ID | ord-48fab08712d94deebfc8aa9ab8fe1b9f |
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| Source note | uspto-grants-2001_10 |
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