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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 380037Erstellt: 26. Oktober 2026

Hydrochloric Acid → 3-Bromo-5-trifluoromethylbenzenesulfonamide

https://huagongshe.com/reaction/380037

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktSulfur DioxideHCID 1119—
Edukt3-Bromo-5-(trifluoromethyl)anilineHCID 2735880—
EduktMagnesium ChlorideHCID 5360315—
EduktSodium NitriteHCID 23668193—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
Produkt3-Bromo-5-trifluoromethylbenzenesulfonamideHCID 21895504—

Reaktionsbedingungen

Temperatur-5 °C

Reaktionsschritte

3-Amino-5-bromobenzotrifluoride was added to concentrated hydrochloric acid (20 ml) and cooled to −5° C. A saturated solution of sodium nitrite (3.88 g) in water (4 ml) was dropwise added at such a rate to maintain the temperature below 0° C. Magnesium chloride (8 g) was added (CARE: exotherm) and the resulting mixture added with stirring to a saturated solution of sulfur dioxide in acetic acid (37.5 ml) and toluene (20 ml), containing cupric chloride (2.75 g) at room temperature. The mixture was stirred for 16 hours, poured into water and extracted into toluene. The combined toluene extracts were washed with water, dilute sodium hydrogen carbonate, dried over anhydrous magnesium sulfate and concentrated. The residue was dissolved in tetrahydrofuran (200 ml) and 880 ammonia (50 ml) was added to the solution. The mixture was stirred at room temperature for 4 hours and then concentrated under reduced pressure. The residue was partitioned between water and ethyl acetate. The combined ethyl acetate extracts were dried over anhydrous magnesium sulfate and concentrated to afford the sub-title compound as a solid (4.2 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06300352B1
Quelldatensatzuspto-grants-2001_10
ORD IDord-83fc3015a7f246068e62c58b29320cda
Quellennotizuspto-grants-2001_10