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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 348889Erstellt: 25. Oktober 2026

Thiazole → Methyl 4-(thiazol-2-Yl)benzoate

https://huagongshe.com/reaction/348889

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktThiazoleHCID 9256—
EduktMethyl 4-iodobenzoateHCID 69273—
EduktButyllithiumHCID 178418339—
KatalysatorZincchlorideHCID 3007855—
KatalysatorTetrakis(triphenylphosphine)palladiumHCID 11979704—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktMethyl 4-(thiazol-2-Yl)benzoateHCID 11241445—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a −70° C., stirred solution of thiazole (270 μL, 3.8 mmol) in tetrahydrofuran (10 mL) is added n-butyl lithium (2.6 mL of a 1.6 M solution in hexanes, 4.2 mmol). After 30 min, zinc chloride (11.4 mL of a 1.0 M solution in diethyl ether, 11.4 mmol) is added. The reaction mixture is warmed to 0° C. and methyl 4-iodobenzoate (1 g, 3.8 mmol) and palladium(0) tetrakis(triphenylphosphine) (530 mg, 0.4 mmol) are added. The reaction mixture is heated at 70° C. for 20 h under argon, cooled to room temperature, and then partitioned between ethyl acetate and water. The organic layer is washed with water, and brine, dried (sodium sulfate), filtered, and concentrated under reduced pressure. Purification by flash column chromatography (3:1 hexanes/ethyl acetate) yields the title compound. 1H NMR (300 MHz, CDCl3) δ 8.14–8.03 (m, 4H), 7.93–7.92 (m, 1H), 7.42–7.41 (m, 1H), 3.95 (s, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07176242B2
Quelldatensatzuspto-grants-2007_02
ORD IDord-2bac21ef6e944361a45ad2faa71ba177
Quellennotizuspto-grants-2007_02