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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 864713Erstellt: 24. Oktober 2026

Hydrochloric Acid → Methyl 2-(chlorosulfonyl)-6-methylbenzoate

https://huagongshe.com/de/reaction/864713

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktSulfur DioxideHCID 1119—
EduktBenzoic acid, 2-amino-6-methyl-, methyl esterHCID 583916—
EduktChloride dihydrateHCID 21226388—
EduktSodium NitriteHCID 23668193—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelWaterHCID 962—
ProduktMethyl 2-(chlorosulfonyl)-6-methylbenzoateHCID 15934071—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

The methyl 6-methylanthranilate so prepared (4.23 g, 0.026 mol) was dissolved in 25 ml of acetic acid and the solution cooled to 0° C. Concentrated hydrochloric acid (45 ml) was added to produce a tan slurry. A solution of 1.89 g (0.027 mol) of sodium nitrite in 8 ml water was added dropwise with stirring, the resulting orange solution was stirred at 0° C. for 1 hour and then added in 6 portions to a mixture of 2.18 g (0.013 mol) of cuptic chloride dihydrate and sulfur dioxide (6.3 g) in 33 ml of acetic acid and 6 ml of water at 0° C. The dark green solution was stirred at room temperature overnight, poured into 300 ml of ice-water, and the solid which separated was collected and dried by suction to provide 1.11 g of methyl 2-chlorosulfonyl-6-methylbenzoate which was immediately added to 100 ml of ice cold ammonium hydroxide and stirred at room temperature overnight. The solution was acidified to pH 1 with concentrated hydrochloric acid, and the resulting precipitate was collected and air-dried to provide 729 mg (12%) of 4-methylsaccharin, mp 224°-226° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05563163
Quelldatensatzuspto-grants-1996_10
ORD IDord-0a4306bb8b90444f8364117aebdc5e80
Quellennotizuspto-grants-1996_10