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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSulfuric AcidHCID 1118—
ReactantIodic acidHCID 24345—
ReactantSodium ThiosulfateHCID 24477—
ReactantEthyl 2-methyl-1,3-thiazole-4-carboxylateHCID 293353—
SolventAcetic AcidHCID 176—
SolventCarbon TetrachlorideHCID 5943—
Product5-Iodo-2-methyl-thiazole-4-carboxylic acid ethyl esterHCID 6885131646.3%

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07544704B2
Source datasetuspto-grants-2009_06
ORD IDord-2fa0b58ac72f47f0946d6fcad0ebf080
Source noteuspto-grants-2009_06