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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2246071Generated: October 27, 2026

Tert-Butyl nitrite → Ethyl 5-iodothiazole-4-carboxylate

https://huagongshe.com/reaction/2246071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-Butyl nitriteHCID 10906—
ReactantEthyl 2-amino-5-iodo-1,3-thiazole-4-carboxylateHCID 45117588—
SolventDimethylformamideHCID 6228—
SolventSodium chloride; waterHCID 57417360—
ProductEthyl 5-iodothiazole-4-carboxylateHCID 5970506950.1%

Reaction Steps

A solution of 10.68 g of 2-amino-4-ethoxycarbonyl-5-iodothiazole in 140 ml of DMF was cooled in ice under an argon atmosphere. t-Butylnitrite (6.15 ml) was added to the cooled solution, and the mixture was stirred at room temperature for 30 min. The reaction solution was poured into brine, and the mixture was extracted three times with ethyl acetate. The organic layers were combined, followed by washing three times with brine. The organic layer was dried over anhydrous magnesium sulfate, was filtered, and was 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 5.08 g of 4-ethoxycarbonyl-5-iodothiazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07687490B2
Source datasetuspto-grants-2010_03
ORD IDord-66f8547db03d453d95e5c28d37c8bdf1
Source noteuspto-grants-2010_03