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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113022Generated: October 26, 2026

Potassium Carbonate → 2-(4-Benzo[1,3]dioxol-5-yl-phenoxymethyl)-thiazole-4-carboxylic acid

https://huagongshe.com/reaction/2113022

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(2H-1,3-benzodioxol-5-yl)boronic acidHCID 2734371—
Reactant2-(4-Iodo-phenoxymethyl)-thiazole-4-carboxylic acid ethyl esterHCID 57643350—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product2-(4-Benzo[1,3]dioxol-5-yl-phenoxymethyl)-thiazole-4-carboxylic acidHCID 11696098—

Reaction Steps

A solution of 2-(4-iodo-phenoxymethyl)-thiazole-4-carboxylic acid ethyl ester (of intermediate 2; 75 mg, 0.2 mmol) in dioxane (4 mL) was added to a reaction tube containing 3,4-methylenedioxybenzeneboronic acid (ASDI Incorporated, Newark, Del.; 100 mg, 0.6 mmol). A solution of potassium carbonate (80 mg, 0.6 mmol) in water (0.4 mL) was added and the mixture was degassed. A solution of bis(tricyclohexylphosphine)-palladium (available from Strem Chemicals, Inc., Newburyport, Mass.; 7 mg, 0.01 mmol) in dioxane (0.5 mL) was added and the tube was heated in a microwave oven at 170 degrees for 25 min. The solution was acidified, filtered through silica gel, evaporated, and triturated with aqueous methanol to give 2-(4-benzo[1,3]dioxol-5-yl-phenoxymethyl)-thiazole-4-carboxylic acid. Mass spectrum MH+=356.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07524870B2
Source datasetuspto-grants-2009_04
ORD IDord-6e775657c3374bd095aa9526d04cc23c
Source noteuspto-grants-2009_04