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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2366067Generated: October 31, 2026

4-Ethylpyridin-2-amine → HCID 55279394, compound

https://huagongshe.com/reaction/2366067

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Ethylpyridin-2-amineHCID 118425—
ReactantSulfuric acid, mixt. with nitric acidHCID 71777668—
CatalystZincHCID 23994—
SolventSulfuric AcidHCID 1118—
SolventSodium HydroxideHCID 14798—
ProductHCID 55279394HCID 5527939477%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 5 g (40.9 mmol) of 4-ethylpyridin-2-amine in 10 mL of concentrated H2SO4 at 0° C. are added 8 mL of an H2SO4/HNO3 mixture (1/1) at a temperature of between 0 and 10° C., and stirring is maintained for 1 hour at 0° C. The reaction medium is then poured onto 100 g of ice and the white precipitate obtained is filtered off and washed successively with 10 mL of water, 10 mL of Et2O and 10 mL of pentane. The solid obtained is taken up in 100 mL of 10N NaOH at 0° C., 7.76 g (187 mmol) of zinc powder are added and the reaction medium is then stirred for 3 hours at 0° C. The reaction medium is then filtered through Celite and the filtrate is extracted with EtOAc (3×200 mL). The organic phases are combined, dried over Na2SO4, filtered and then concentrated under reduced pressure. 4.3 g of 4-ethyl-2-hydrazinopyridine are obtained in the form of a red oil, which is used without further purification in the following step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697731B2
Source datasetuspto-grants-2014_04
ORD IDord-4f1ec157fe36427f8daf4fe09f4e077d
Source noteuspto-grants-2014_04