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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 554756Erstellt: 24. Oktober 2026

Sulfur Dioxide → Methyl 2-chloro-5-sulfamoylbenzoate

https://huagongshe.com/de/reaction/554756

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfur DioxideHCID 1119—
EduktMethyl 5-Amino-2-chlorobenzoateHCID 5200412—
EduktSodium NitriteHCID 23668193—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelHydrochloric AcidHCID 313—
ProduktMethyl 2-chloro-5-sulfamoylbenzoateHCID 13960349—

Reaktionsbedingungen

Temperatur-5 °C

Reaktionsschritte

To methyl 5-amino-2-chlorobenzoate (16.2 g) in concentrated hydrochloric acid (40 ml)/acetic acid (120 ml) suspension, a sodium nitrite (7.6 g) aqueous solution (20 ml) was added under ice cooling and the mixture was stirred at that temperature for 45 minutes. Next, the inside temperature of the reaction vessel was cooled to −5° C., copper (II) chloride 2-hydrate (3.7 g) and a 21% sulfur dioxide in acetic acid solution (60 ml) were added, and the mixture was raised to room temperature and stirred at 12 hours. Under ice cooling, distilled water was added to the reaction solution, the mixture was stirred at that temperature for 30 minutes, and the precipitate was collected by filtration. The filtrate was dissolved in tetrahydrofuran (50 ml), 28% ammonia water (10 ml) was added under ice cooling, and the mixture was stirred at that temperature for 15 minutes. The tetrahydrofuran was distilled off in vacuo, then ethyl acetate/hexane was added. The precipitate was collected by filtration to obtain the title compound (10.9 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08049006B2
Quelldatensatzuspto-grants-2011_11
ORD IDord-78cafef48deb42928537a0e88bad9a03
Quellennotizuspto-grants-2011_11