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HRID 383944作成日:2026年10月26日

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

https://huagongshe.com/reaction/383944

反応式

関与物質

役割名称HCID仕込み量
反応物N-bromobutanimideHCID 67184—
反応物Ethyl 2-methyl-1,3-thiazole-4-carboxylateHCID 293353—
反応物Sodium BicarbonateHCID 516892—
溶媒AcetonitrileHCID 6342—
生成物Ethyl 5-bromo-2-methylthiazole-4-carboxylateHCID 5929123940.1%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08367696B2
出典データセットuspto-grants-2013_02
ORD IDord-a8c009059a5f495dae254bba06320339
出典メモuspto-grants-2013_02