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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 394778Erstellt: 24. Oktober 2026

Ethyl benzoylacetate → Ethyl 2-amino-4-phenyl-1,3-thiazole-5-carboxylate

https://huagongshe.com/de/reaction/394778

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl benzoylacetateHCID 7170—
EduktThioureaHCID 2723790—
EduktHydroxy tosyloxy iodobenzeneHCID 21918218—
LösungsmittelAcetonitrileHCID 6342—
ProduktEthyl 2-amino-4-phenyl-1,3-thiazole-5-carboxylateHCID 7323975,9%

Reaktionsbedingungen

Temperatur65 °C

Reaktionsschritte

To a solution of ethyl 3-phenyl-3-oxopropionate (5.0 g, 26.0 mmol) in 100 mL of acetonitrile was added hydroxy(tosyloxy)iodobenzene (11.2 g, 28.6 mmol). The resulting suspension was stirred at 65° C. for 1 h at which time the reaction was a homogeneous solution. Thiourea (2.2 g, 28.6 mmol) was added and stirring was continued at 65° C. for 2 h. The mixture was cooled and concentrated, and the residue was taken up in ethyl acetate, washed with saturated aq Na2CO3 and brine, dried (MgSO4) and concentrated. The residue was triturated with ethyl ether to afford 4.9 g (70%) of the title compound as a yellow solid. 1H NMR (CDCl3) d 7.65 (m, 2H), 7.39 (m, 3H), 5.98 (broad s, 2H), 4.18 (q, 2H), 1.22 (t, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06602895B2
Quelldatensatzuspto-grants-2003_08
ORD IDord-0f7ec75b59b14721884206e1f615b0c5
Quellennotizuspto-grants-2003_08