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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 847770Generated: October 25, 2026

3-Ethoxy-2-methyl-6-nitropyridine → 5-Ethoxy-6-methylpyridin-2-amine

https://huagongshe.com/reaction/847770

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Ethoxy-2-methyl-6-nitropyridineHCID 12875016—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product5-Ethoxy-6-methylpyridin-2-amineHCID 1287501790.8%

Reaction Steps

18.2 g of the nitro compound obtained above was suspended in 300 ml of ethanol, which was reduced over 2 g of 5% palladium black under atmospheric pressure. After reaction, the catalyst was filtered off and the solvent was evaporated in vacuo. The residue was crystallized from benzene to obtain 13.8 g of 3-ethoxy-2-methyl-6-aminopyridine (Compound IV where R2 =C2H5), m.p. 98°-99° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04293695
Source datasetuspto-grants-1981_10
ORD IDord-7546caff650d435fac3441641d4fbc59
Source noteuspto-grants-1981_10