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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 737171Erstellt: 25. Oktober 2026

1,4-Diacetylbenzene → 1-[4-(2-Amino-thiazol-4-yl)-phenyl]-ethanone

https://huagongshe.com/reaction/737171

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,4-DiacetylbenzeneHCID 13888—
EduktBromineHCID 24408—
EduktCarbonyl bromideHCID 79057—
EduktSodium AcetateHCID 517045—
EduktThioureaHCID 2723790—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelEthanolHCID 702—
Produkt1-[4-(2-Amino-thiazol-4-yl)-phenyl]-ethanoneHCID 86616431—

Reaktionsschritte

A solution of 1-(4-Acetyl-phenyl)-ethanone (8.1 g, 5 mmol), in HOAc (50 mL) at 60° C. was treated with bromine (1 eq., 0.26 mL) dropwise over 10 minutes. After 5 more minutes the reaction was cooled, the acetic acid was removed, ethyl acetate (50 mL) was added and then removed to get drive off the remainder of the acetic acid. The crude bromo ketone was then dissolved in ethanol (30 mL) with NaOAc (1.1 g) and thiourea (1 eq., 375 mg) was added. The suspension was stirred at room temperature for 15 hours. The solvents were removed and the resulting mixture was redissolved in 5 ml of 90% DMF, 10% water with 0.1% TFA and purified by reverse phase HPLC to give the product. MS: 219.1 (M+H−).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07595398B2
Quelldatensatzuspto-grants-2009_09
ORD IDord-bf1e3eb4baff409c84040f25d0325913
Quellennotizuspto-grants-2009_09