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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 477598Erstellt: 24. Oktober 2026

Water → 3-ethoxycarbonylmethyl-6-fluoro-5-nitro-2(3H)-benzothiazolone

https://huagongshe.com/de/reaction/477598

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktEthyl bromoacetateHCID 7748—
EduktSodium hydrideHCID 24758—
Edukt6-fluoro-5-nitro-2(3H)-benzothiazoloneHCID 13957955—
LösungsmittelDimethylformamideHCID 6228—
Produkt3-ethoxycarbonylmethyl-6-fluoro-5-nitro-2(3H)-benzothiazoloneHCID 1401424425%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

50% Oily sodium hydride (0.21 g) was suspended in N,N-dimethylformamide (5 ml), and the resultant suspension was cooled to 0° C. 6-Fluoro-5-nitro-2(3H)-benzothiazolone (1.0 g) was portionwise added thereto at 0° C., and the mixture was stirred at the same temperature for 30 minutes. Ethyl bromoacetate (0.86 g) was added to the reaction mixture at 0° C., and the temperature was gradually elevated to a temperature of 50° to 60° C., followed by stirring at that temperature for 3 hours. Water was added to the mixture, which was extracted with ethyl acetate. The extract was washed with water, dried and concentrated. The residue was purified by silica gel thin layer chromatography with a mixture of ethyl acetate and toluene (1:9) to give 0.35 g of 3-ethoxycarbonylmethyl-6-fluoro-5-nitro-2(3H)-benzothiazolone, m.p., 139.0°-140.0° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04888428
Quelldatensatzuspto-grants-1989_12
ORD IDord-33779e788a05417badbe4024f628ef3d
Quellennotizuspto-grants-1989_12