HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1984662Generated: October 26, 2026
Iodine → 5-Iodo-2-methyl-thiazole-4-carboxylic acid ethyl ester
https://huagongshe.com/reaction/1984662
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodine | HCID 807 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Iodic acid | HCID 24345 | — |
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | Ethyl 2-methyl-1,3-thiazole-4-carboxylate | HCID 293353 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 5-Iodo-2-methyl-thiazole-4-carboxylic acid ethyl ester | HCID 68851316 | 46.3% |
Reaction Steps
To a solution of ethyl 2-methylthiazole-4-carboxylate (11.2 g, 65.4 mmol) in acetic acid (200 mL) were added sulfuric acid (30%, 20 mL), carbontetrachloride (30 mL), iodine (33.2 g, 131 mmol) and iodic acid (11.5 g, 65.4 mmol) and the resulting reaction mixture was stirred for 19 h at 80° C. After addition of aqueous sodium thiosulfate (1 M, 500 mL) it was extracted with ethyl acetate (1000 mL). The combined organic layers were washed with aqueous sodium carbonate (saturated, 1000 mL), dried over sodium sulfate and concentrated. Purification by chromatography (SiO2, heptane:ethyl acetate=95:5 to 20:80) afforded the title compound (9.00 g, 37%) as a white crystalline solid. MS: m/e=298.1 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07544704B2 |
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| Source dataset | uspto-grants-2009_06 |
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| ORD ID | ord-2fa0b58ac72f47f0946d6fcad0ebf080 |
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| Source note | uspto-grants-2009_06 |
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