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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 617265Erstellt: 25. Oktober 2026

Ethyl Acetate → 7-Bromo-5-nitrobenzothiazole

https://huagongshe.com/reaction/617265

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
EduktNitrosylsulfuric acidHCID 82157—
EduktPhosphinic AcidHCID 4124402—
Edukt7-Bromo-5-nitrobenzo[d]thiazol-6-amineHCID 22728034—
LösungsmittelSulfuric AcidHCID 1118—
Produkt7-Bromo-5-nitrobenzothiazoleHCID 2272803189%

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

To a solution of 5 -nitro-6-amino-7-bromobenzothiazole (1.0 g, 3.7 mmol) in 4 mL of sulfuric acid was added nitrososulfuric acid (1.2 g, 9.5 mmol) in a portion. The resulting reaction mixture was stirred for 12 h at 25° C. The reaction mixture was then cooled to 0° C. and 1 mL of H3PO2 was added into the solution. It was stirred for 12 h at another 25° C. and for 2 h at 50° C. The reaction mixture was then poured into EtOAc and washed with aq. NaHCO3. Organic layer was dried over Na2SO4 and concentrated in vacuo to provide an oil (0.85 g, 3.2 mmol, 89%), whicn was characterized as the desired product(>95% pure) and subjected to a following reaction without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05948804
Quelldatensatzuspto-grants-1999_09
ORD IDord-1139423dfe2243848cb7bac00d0e8101
Quellennotizuspto-grants-1999_09