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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348889Generated: October 25, 2026

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

https://huagongshe.com/reaction/348889

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiazoleHCID 9256—
ReactantMethyl 4-iodobenzoateHCID 69273—
ReactantButyllithiumHCID 178418339—
CatalystZincchlorideHCID 3007855—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 4-(thiazol-2-Yl)benzoateHCID 11241445—

Reaction Conditions

Temperature0 °C

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176242B2
Source datasetuspto-grants-2007_02
ORD IDord-2bac21ef6e944361a45ad2faa71ba177
Source noteuspto-grants-2007_02