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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 383944Erstellt: 25. Oktober 2026

N-bromobutanimide → Ethyl 5-bromo-2-methylthiazole-4-carboxylate

https://huagongshe.com/reaction/383944

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-bromobutanimideHCID 67184—
EduktEthyl 2-methyl-1,3-thiazole-4-carboxylateHCID 293353—
EduktSodium BicarbonateHCID 516892—
LösungsmittelAcetonitrileHCID 6342—
ProduktEthyl 5-bromo-2-methylthiazole-4-carboxylateHCID 5929123940,1%

Reaktionsschritte

To a solution of ethyl 2-methyl-1,3-thiazole-4-carboxylate (14.53 g) in MeCN (150 mL) was added NBS (22.66 g), followed by heating under reflux for 3 hours. To the reaction mixture was added NBS (7.55 g), followed by heating under reflux for 2 hours. Under ice-cooling, to the reaction mixture was added a saturated aqueous NaHCO3 solution, followed by stirring for 5 minutes, and then extraction with EtOAc. The organic layer was dried over MgSO4 and then concentrated under reduced pressure. The residue obtained was purified by silica gel column chromatography (hexane:EtOAc=from 100:0 to 60:40) to obtain ethyl 5-bromo-2-methyl-1,3-thiazole-4-carboxylate (8.52 g) as a yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08367696B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-a8c009059a5f495dae254bba06320339
Quellennotizuspto-grants-2013_02