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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2112994Generated: October 26, 2026

4-Iodophenol → 2-(4-Iodo-phenoxymethyl)-thiazole-4-carboxylic acid ethyl ester

https://huagongshe.com/reaction/2112994

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-IodophenolHCID 10894—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 2-(bromomethyl)-1,3-thiazole-4-carboxylateHCID 11043146—
SolventAcetoneHCID 180—
Product2-(4-Iodo-phenoxymethyl)-thiazole-4-carboxylic acid ethyl esterHCID 5764335065%

Reaction Steps

Ground potassium carbonate (3.4 g, 24.6 mmol) was added to a solution of 2-bromomethyl-thiazole-4-carboxylic acid ethyl ester (12.83 g, 56 mmol; from Step 1 above) and 4-iodophenol (5.5 g, 25 mmol; available from Aldrich Chemical Company, Inc., Milwaukee, Wis.) in acetone (440 mL). The reaction mixture was heated at reflux for 15 h and then it was filtered and water was added to the filtrate until it turned cloudy. The filtrate was left on ice and then the resulting white solid was filtered off, washed with acetone/hexanes (2:1) and dried to give 2-(4-iodo-phenoxymethyl) -thiazole-4-carboxylic acid ethyl ester (5.6 g, 65%) as a white solid. 1HNMR (CDCl3): δ 1.4 (t, 3H, J=7 Hz), 4.46 (q, 2H, J=7 Hz), 5.4 (s, 2H), 6.7 (d, 2H, J=9 Hz), 7.6 (d, 2H, J=9 Hz), 8.2 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07524870B2
Source datasetuspto-grants-2009_04
ORD IDord-3d7f91870658478b9bc816d97290f742
Source noteuspto-grants-2009_04