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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 978632Generated: October 31, 2026

Maleic Anhydride → 3-(2-Chloro-5-nitrophenylsulphonyl)-propionic acid

https://huagongshe.com/reaction/978632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMaleic AnhydrideHCID 7923—
ReactantBenzenesulfinic acid, 2-chloro-5-nitro-, sodium salt (1:1)HCID 111522—
ReactantSodium BicarbonateHCID 516892—
SolventWaterHCID 962—
Product3-(2-Chloro-5-nitrophenylsulphonyl)-propionic acidHCID 1375025780.9%

Reaction Conditions

Temperature100 °C

Reaction Steps

36 g of sodium 2-chloro-5-nitrobenzenesulphinate, 12.6 g of solid sodium hydrogen carbonate and 22.5 g of maleic anhydride are heated at 100° C. in 250 ml of water for 3 hours. After cooling down, a further 12.6 g of sodium hydrogencarbonate and 22.5 g of maleic anhydride are then added. After a further 5 hours of stirring at 100° C., the cooled, weakly acid reaction mixture is filtered with suction. The filter is cake at 50° C. in 300 ml of water, and the suspension is cooled down to 20° C. and is filtered again with suction. Drying gives 35.1 g of 3-(2-chloro-5-nitrophenylsulphonyl)-propionic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04665179
Source datasetuspto-grants-1987_05
ORD IDord-9ec27545afc14c46827e073c8719b23b
Source noteuspto-grants-1987_05