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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 277009Generated: October 26, 2026

Sodium Hydroxide → Furan-2-carboxylic acid (1-amino-2-benzenesulfonyl-ethylidene)-hydrazide

https://huagongshe.com/reaction/277009

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant2-Furancarboxylic acid, hydrazideHCID 18731—
ReactantSodium BicarbonateHCID 516892—
Reactant2-(Phenylsulfonyl)-ethanimidic acid ethyl ester hydrochlorideHCID 70089441—
SolventChloroformHCID 6212—
ProductFuran-2-carboxylic acid (1-amino-2-benzenesulfonyl-ethylidene)-hydrazideHCID 86757843—

Reaction Steps

A suspension of 85.0 g (0.32 mol) 2-(phenylsulfonyl)-ethanimidic acid ethyl ester hydrochloride in 700 ml chloroform was treated with 320 ml 1N aqueous sodium hydoxide. 100 ml of a saturated aqueous sodiumbicarbonate solution was added and the mixture was extracted with chloroform. The extracts were combined and dried with sodium sulfate and the solvents were distilled off under reduced pressure. The resulting colorless oil was stirred together with 42.6 g (0.34 mol) 2-furancarboxylic acid hydrazide in 600 ml chloroform for 24 hours at 50° C. The resulting precipitate was filtered off and dried. A quantitative yield of furan-2-carboxylic acid (1-amino-2-benzenesulfonyl-ethylidene)-hydrazide was obtained as pale crystals, mp. 195° C. (decomposition), MS m/e (%): 308 (M+H+, 100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06355653B1
Source datasetuspto-grants-2002_03
ORD IDord-851ab4618392489f911aff3525372778
Source noteuspto-grants-2002_03