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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 892739Generated: October 25, 2026

Hydrazine hydrate (1:1) → 4-(Quinolin-2-ylmethoxy)aniline

https://huagongshe.com/reaction/892739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant2-[(4-Nitrophenoxy)methyl]quinolineHCID 13770360—
CatalystNickelHCID 935—
SolventMeOH tetrahydrofuranHCID 21899815—
Product4-(Quinolin-2-ylmethoxy)anilineHCID 2747569—

Reaction Conditions

Temperature35 °C

Reaction Steps

117.8 g (0.42 mol) of 2-(4-nitrophenoxymethyl)quinoline were dissolved in 1 l of methanol/tetrahydrofuran (1:1). About 5 g of Raney nickel were added and the mixture was warmed to 35° C. 63.1 g (1.26 mol) of hydrazine hydrate were then added dropwise and the mixture was stirred overnight. The residue was filtered off, the solution was concentrated in vacuo and the residue was taken up with methylene chloride. The solution was then washed with water and conc. hydrochloric acid was added to the organic phase. The precipitate which deposited was filtered off, washed with 2N hydrochloric acid and dissolved in water, and the solution was rendered alkaline with 20% strength NaOH. The residue was dried in vacuo.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05120744
Source datasetuspto-grants-1992_06
ORD IDord-2e4cd6db82ee48a7960663130937bec4
Source noteuspto-grants-1992_06