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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2257137Generated: October 26, 2026

Hydrochloric Acid → Methyl 3-hydrazinylbenzoate hydrochloride

https://huagongshe.com/reaction/2257137

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSulfurous AcidHCID 1100—
ReactantBenzoic acid, 3-amino-, methyl esterHCID 78274—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
ProductMethyl 3-hydrazinylbenzoate hydrochlorideHCID 23285088—

Reaction Steps

A solution of 5.75 g of sodium nitrite in 30 ml of water was dropwise added to a solution of 11.7 g of methyl 3-aminobenzoate and 20 ml of concentrated hydrochloric acid in 200 ml of water, at about 0° C. with cooling with ice-methanol. The mixture was stirred at the same temperature for 5 minutes. The mixture was then added to 650 ml of a 6% aqueous sulfurous acid solution being ice-cooled. The resulting mixture was stirred at 50°-60° C. for 2 days. The reaction mixture was allowed to cool and then extracted with ethyl acetate. The aqueous layer was made basic with an aqueous sodium hydroxide solution and extracted with ethyl acetate. The extract was washed with water and an aqueous sodium chloride solution in this order, then dried with anhydrous sodium sulfate, and concentrated under reduced pressure. To the residue was added ethanol. The mixture was made acidic with concentrated hydrochloric acid and then concentrated under reduced pressure. To the residue was added a slight amount of ethanol. The resulting insolubles were collected by filtration, washed with ethanol, and dried to obtain 3.1 g of methyl 3-hydrazinobenzoate hydrochloride as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05656642
Source datasetuspto-grants-1997_08
ORD IDord-7d9b2fc3fe97423c8074ad97913c51fe
Source noteuspto-grants-1997_08