Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1799677Generated: October 31, 2026

Diiodomethane → 2-Iodo-thiazole-4-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1799677

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiiodomethaneHCID 6346—
ReactantTert-Butyl nitriteHCID 10906—
ReactantEthyl 2-aminothiazole-4-carboxylateHCID 73216—
SolventAcetonitrileHCID 6342—
SolventSodium chloride; waterHCID 57417360—
Product2-Iodo-thiazole-4-carboxylic acid ethyl esterHCID 6847277865.8%

Reaction Steps

A solution of 6.0 ml of t-butyl nitrite in 120 ml of acetonitrile was cooled in ice under an argon atmosphere, and 9.64 g of diiodomethane and 5.16 g of 2-amino-4-ethoxycarbonylthiazole were added to the cooled solution. The mixture was stirred at room temperature for one hr, brine was added thereto, and the mixture was extracted twice with ethyl acetate. The organic layers were combined, were washed twice with brine, were dried over anhydrous magnesium sulfate, were filtered, and were concentrated under the reduced pressure. The residue was purified by column chromatography on silica gel (hexane:ethyl acetate=5:1 to 3:1) to give 5.58 g of 4-ethoxycarbonyl-2-iodothiazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08344154B2
Source datasetuspto-grants-2013_01
ORD IDord-294a6934534948b2b289adeefa48dfdf
Source noteuspto-grants-2013_01