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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | 2-[(4-Nitrophenoxy)methyl]quinoline | HCID 13770360 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | MeOH tetrahydrofuran | HCID 21899815 | — |
| Product | 4-(Quinolin-2-ylmethoxy)aniline | HCID 2747569 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05120744 |
|---|
| Source dataset | uspto-grants-1992_06 |
|---|
| ORD ID | ord-2e4cd6db82ee48a7960663130937bec4 |
|---|
| Source note | uspto-grants-1992_06 |
|---|