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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 737168Erstellt: 26. Oktober 2026

4-Acetylbenzoic Acid → 4-(2-Amino-1,3-thiazol-4-yl)benzoic acid

https://huagongshe.com/reaction/737168

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Acetylbenzoic AcidHCID 11470—
EduktBromineHCID 24408—
EduktCarbonyl bromideHCID 79057—
EduktSodium AcetateHCID 517045—
EduktThioureaHCID 2723790—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelEthanolHCID 702—
Produkt4-(2-Amino-1,3-thiazol-4-yl)benzoic acidHCID 613179—

Reaktionsschritte

A solution of 4-acetyl-benzoic acid (10 g, 61 mmol), in HOAc (400 mL) at 55° C. was treated with bromine (1 eq., 3.12 mL) dropwise over 10 minutes. After 90 minutes the reaction was cooled, the acetic acid was removed, ethyl acetate (50 mL) was added and then removed to get rid of the remainder of the acetic acid. The crude bromo ketone was then dissolved in ethanol (200 mL) with NaOAc (12 g) and thiourea (1 eq. 4.4 g) was added. The suspension was stirred at room temperature for 15 hours. The solvents were removed and the solids washed with water (3×100 mL) then ether:ethanol (4:1, 3×100 mL) and dried to give the product as a tan solid. MS: 221.2 (M+H+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07595398B2
Quelldatensatzuspto-grants-2009_09
ORD IDord-d29e033db8d04bd3b35694af9be5cf39
Quellennotizuspto-grants-2009_09