Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1709030Erstellt: 24. Oktober 2026

Potassium Hydroxide → 6-Fluoro-2(3H)-benzothiazolon-5-ylhydrazine

https://huagongshe.com/de/reaction/1709030

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium HydroxideHCID 14797—
Edukt5-amino-6-fluorobenzo[d]thiazol-2(3H)-oneHCID 14458685—
EduktSodium NitriteHCID 23668193—
LösungsmittelHydrochloric AcidHCID 313—
Produkt6-Fluoro-2(3H)-benzothiazolon-5-ylhydrazineHCID 1477163847%

Reaktionsschritte

A suspension of 5-amino-6-fluoro-2(3H)-benzothiazolone (12.98 g) in conc. hydrochloric acid (70 g) was cooled to 0° to 5° C., and a saturated aqueous solution of sodium nitrite (5.08 g) was dropwise added thereto at 0° to 5° C., followed by stirring at the same temperature for 30 minutes. The resultant mixture was cooled to -20° C., and a solution of stannous chloride (28.06 g) in conc. hydrochloric acid (30 g) was added thereto all at once, followed by stirring at 0° C. for 2 hours. The reaction mixture was neutralized with potassium hydroxide, a colloidal substance originated from stannous chloride was removed by celite and the resultant solution was extracted with ethyl acetate. The extract was washed with water, dried over magnesium sulfate and concentrated to give 6-fluoro-2(3H)-benzothiazolon-5-ylhydrazine (6.60 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04946961
Quelldatensatzuspto-grants-1990_08
ORD IDord-72adc180d26f4e7e89bcc32513f87f8e
Quellennotizuspto-grants-1990_08