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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 466789Erstellt: 26. Oktober 2026

Chloroacetic Acid → 2-Chloro-4-(methylsulfonyl)benzoic acid

https://huagongshe.com/reaction/466789

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChloroacetic AcidHCID 300—
EduktHydrochloric AcidHCID 313—
EduktSodium HydroxideHCID 14798—
EduktSodium SulfiteHCID 24437—
Edukt2-Chloro-4-(chlorosulfonyl)benzoic acidHCID 188427—
EduktSodium BicarbonateHCID 516892—
Edukt2-Chloro-4-sulfinylbenzoic acidHCID 86746215—
LösungsmittelWaterHCID 962—
Produkt2-Chloro-4-(methylsulfonyl)benzoic acidHCID 735863105,9%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

A 250 mL round bottom flask equipped with a reflux condenser, thermometer, and magnetic stirrer was charged with 9.2 g (73 mmol) of sodium sulfite, 24.6 g (292 mmol) of sodium bicarbonate and 80 mL of water. The resulting slurry was heated to 50° C., and 20.0 g (70 mmol) of 2-chloro-4-(chlorosulfonyl)benzoic acid was added over 15 minutes. After heating at 50° C. for three hours, chloroacetic acid (10.4 g, 110 mmol) and 5.7 mL (110 mmol) of 50% aqueous sodium hydroxide were added sequentially to the aqueous solution of 2-chloro-4-sulfinylbenzoic acid, and the reaction mixture heated to reflux. After heating for 19 hours, the reaction mixture was allowed to cool to ambient temperature and acidified with dilute HCl. The precipitated solids were collected by filtration, washed with dilute HCl and dried to give 17.4 g of 2-chloro-4-(methylsulfonyl)benzoic acid as a white solid. The solid was assayed at 85% purity, corresponding to an overall yield of 89%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05157150
Quelldatensatzuspto-grants-1992_10
ORD IDord-bd1ad13c0e614bd0b9b7539c51c775b6
Quellennotizuspto-grants-1992_10