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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1534577Generated: October 30, 2026

Ammonia → N-tert-Butyl-3-methylpyridine-2-carboxamide

https://huagongshe.com/reaction/1534577

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantSulfuric AcidHCID 1118—
ReactantTolueneHCID 1140—
Reactant3-Methylpyridine-2-carbonitrileHCID 819928—
SolventWaterHCID 962—
Solventtert-ButanolHCID 6386—
ProductN-tert-Butyl-3-methylpyridine-2-carboxamideHCID 5463796—

Reaction Conditions

Temperature70 °C

Reaction Steps

Suspend 2-cyano-3-methyl pyridine (400 g) in t-butanol (800 mL) and heat to 70° C. Add concentrated sulphuric acid (400 mL) dropwise over 45 minutes. Maintain the temperature at 75° C., until the reaction is complete, and for an additional 30 minutes. Dilute the mixture with water (400 mL), charge with toluene (600 mL) and bring to pH 10 with concentrated aqueous ammonia. Maintain the temperature at 50°-55° C. during the work up. Separate the toluene phase, and reextract the aqueous layer. Combine toluene phases and wash with water. Remove the toluene to yield the title compound N-(1,1-dimethylethyl)-3-methyl-2-pyridine carboxamide, as an oil, from which solid product is crystallized. (Yield 97%, as determined by an internal standard assay with gas chromatography).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05089496
Source datasetuspto-grants-1992_02
ORD IDord-357212c99f4e489fb6b6fde4c5d3a3ec
Source noteuspto-grants-1992_02