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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 236270Generated: October 26, 2026

Acetohydrazide → 5-(p-Chlorophenyl)-2-furoic Acid 1-Acetylhydrazine

https://huagongshe.com/reaction/236270

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetohydrazideHCID 14039—
Reactant5-(4-Chlorophenyl)-2-furoic acidHCID 726693—
SolventChloroformHCID 6212—
SolventThionyl ChlorideHCID 24386—
Product5-(p-Chlorophenyl)-2-furoic Acid 1-AcetylhydrazineHCID 7043398064%

Reaction Steps

A mixture of 111.5 g (0.50 mole) of 5-(p-chlorophenyl)-2-furoic acid in 500 ml of thionyl chloride was heated at refluxed for 13/4 hr. After slight cooling, the reaction mixture was filtered and the filtrate was concentrated in a water bath at reduced pressure to a creamy solid. The solid was dissolved in 400 ml of chloroform. To this chloroform solution under stirring at room temperature was added a suspension of 74 g (1.0 mole) of acetylhydrazine in 900 ml of chloroform. Addition was completed in about 20 min. White creamy solid separated fairly readily while the temperature rose to about 45°. The mixture was allowed to stir at ambient temperature overnight. The mixture was filtered and the solid was washed with chloroform and air dried. The solid was further triturated with water, filtered, washed with water again and air dried. The yield of crude product was 120 g (89%). Recrystallization from ethyl acetate gave 95 g of product, m.p. 206°-208°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04643996
Source datasetuspto-grants-1987_02
ORD IDord-734103e3ef174dbd913d36031004da25
Source noteuspto-grants-1987_02