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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1437258Generated: November 1, 2026

Hydrazine hydrate (1:1) → 2-Hydrazinyl-5-methoxypyridine

https://huagongshe.com/reaction/1437258

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant2-Chloro-5-methoxypyridineHCID 15169000—
Product2-Hydrazinyl-5-methoxypyridineHCID 23090245—

Reaction Steps

The above-obtained 2-chloro-5-methoxypyridine (4.0 g) in hydrazine monohydrate (30 mL) was stirred at 100° C. for 24 hours, and then cooled in air. The reaction solvent was removed under reduced pressure, and the residue was partitioned by use of chloroform and aqueous 1N sodium hydroxide. The organic layer was dried over magnesium sulfate anhydrate, followed by filtration. The solvent was removed under reduced pressure, to thereby give 2-hydrazino-5-methoxypyridine as an oily product (705 mg, 18%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622471B2
Source datasetuspto-grants-2009_11
ORD IDord-5ef3b5688d254272ae3d74ff557b17fd
Source noteuspto-grants-2009_11