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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Iodophenol | HCID 10894 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 2-(bromomethyl)-1,3-thiazole-4-carboxylate | HCID 11043146 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-(4-Iodo-phenoxymethyl)-thiazole-4-carboxylic acid ethyl ester | HCID 57643350 | 65% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07524870B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-3d7f91870658478b9bc816d97290f742 |
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| Source note | uspto-grants-2009_04 |
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