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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2073229Generated: October 30, 2026

Hydrazine hydrate (1:1) → Methyl 4-hydrazinyl-3-nitrobenzoate

https://huagongshe.com/reaction/2073229

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantMethyl 4-chloro-3-nitrobenzoateHCID 735797—
SolventEthanolHCID 702—
ProductMethyl 4-hydrazinyl-3-nitrobenzoateHCID 1308828485%

Reaction Steps

80 ml of hydrazine hydrate were poured into the suspension of 172.5 g of methyl 4-chloro-3-nitrobenzoate in 1600 ml of abs. ethanol under stirring, then the reaction mixture was refluxed while stirring for 45 minutes. The starting material dissolved and the product started to precipitate. After cooling down, the product was filtered by suction, washed with abs. ethanol and water successively until it became free from chloride ion. Thus, 4-methoxycarbonyl-2-nitrophenylhydrazine (143.6 g, 85%) was obtained as yellow crystals m.p.: 169°-171° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04916149
Source datasetuspto-grants-1990_04
ORD IDord-972664d61db6433a97c6b3ba196b2c06
Source noteuspto-grants-1990_04