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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thiazole | HCID 9256 | — |
| Reactant | Methyl 4-iodobenzoate | HCID 69273 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 4-(thiazol-2-Yl)benzoate | HCID 11241445 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07176242B2 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-2bac21ef6e944361a45ad2faa71ba177 |
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| Source note | uspto-grants-2007_02 |
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