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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1605742Generated: November 2, 2026

p-Toluenesulfonic acid → HCID 20367264, compound

https://huagongshe.com/reaction/1605742

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactantbeta-Aminobeta-ethoxyacrylic acid ethyl esterHCID 278451—
Reactant[(2,3-Dichlorophenyl)methyl]hydrazineHCID 20367233—
SolventEthanolHCID 702—
ProductHCID 20367264HCID 20367264—

Reaction Steps

16.7 g of β-amino-β-ethoxyacrylic acid ethyl ester and 1 g of p-toluenesulphonic acid were dissolved in 100 ml of ethanol and 20.2 g of 2,3-dichlorobenzylhydrazine were added. After standing overnight at room temperature, the precipitate which had formed was filtered off and dissolved in 2 N sodium hydroxide solution. The alkaline solution was again extracted with ether and subsequently slightly acidified with dilute acetic acid. Hereupon the compound identified above precipitated and after recrystallisation from ethanol the melting point was 161°-162°C. Yield: 11 g (40%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03950528
Source datasetuspto-grants-1976_04
ORD IDord-220f87ad056849bb8b9ca14eb4b65646
Source noteuspto-grants-1976_04