HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1191956Generated: November 2, 2026
Potassium Chloride → Tert-butyl 2-(4-(thiazol-2-yl)phenoxy)acetate
https://huagongshe.com/reaction/1191956
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Chloride | HCID 4873 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-Bromothiazole | HCID 76430 | — |
| Reactant | Tert-butyl 2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)acetate | HCID 59852411 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Tert-butyl 2-(4-(thiazol-2-yl)phenoxy)acetate | HCID 86691024 | 95% |
Reaction Steps
To a solution of 2-bromothiazole (265 μL, 2.97 mmol), tert-butyl 2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)acetate (1.19 g, 3.56 mmol), KCl (664.7 mg, 8.91 mmol) in a 4:1 mixture of toluene (20 mL)/EtOH (5 mL) was added an aqueous solution of Na2CO3 2M (11.8 mL). The flask was evacuated and re-filled with nitrogen three times and then, tetrakis(triphenylphosphine)palladium (0) (346.2 mg, 0.30 mmol) was added. The reaction mixture was heated to 100° C. for 4 h. When the reaction was completed, inorganic solids were removed by filtration through Celite® and washing with several portions of dichloromethane, then the solvent was evaporated. The residue was absorbed onto silica then subjected to flash chromatography (SiO2, hexane: ethyl acetate (AcOEt), 9:1) to afford 825.2 mg of de tert-butyl 2-(4-(thiazol-2-yl)phenoxy)acetate as a white solid (95% yield). RMN1H (CDCl3, 400 MHz): δ 7.95-7.86; (m, 2H), 7.81; (d, J=3.3 Hz, 1H), 6.99-6.85; (m, 1H), 4.57; (s, 2H), 1.49; (s, 1H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08680126B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-15fcc509425b4f889b56bbe397f11f0b |
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| Source note | uspto-grants-2014_03 |
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