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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium ChlorideHCID 4873—
ReactantSodium CarbonateHCID 10340—
Reactant2-BromothiazoleHCID 76430—
ReactantTert-butyl 2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)acetateHCID 59852411—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
ProductTert-butyl 2-(4-(thiazol-2-yl)phenoxy)acetateHCID 8669102495%

Reaction Conditions

Temperature100 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680126B2
Source datasetuspto-grants-2014_03
ORD IDord-15fcc509425b4f889b56bbe397f11f0b
Source noteuspto-grants-2014_03