Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1761446Generated: November 1, 2026

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

https://huagongshe.com/reaction/1761446

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 numberUS04826853
Source datasetuspto-grants-1989_05
ORD IDord-fdd17fd03d3a4f56bdef97b787ee58cf
Source noteuspto-grants-1989_05