戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 238656作成日:2026年10月24日

Sodium bis(trimethylsilyl)amide → 1,1-Dimethylethyl 4-(4-ethenyl-2-thiazolyl)-1-piperidinecarboxylate

https://huagongshe.com/ja/reaction/238656

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium bis(trimethylsilyl)amideHCID 2724254—
反応物tert-Butyl 4-(4-formyl-1,3-thiazol-2-yl)piperidine-1-carboxylateHCID 7172298—
触媒Methyltriphenyliphosphonium bromideHCID 74505—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物1,1-Dimethylethyl 4-(4-ethenyl-2-thiazolyl)-1-piperidinecarboxylateHCID 6874364595.2%

反応手順

To a cold (−50° C.) suspension of methyltriphenylphosphonium bromide (1.2 g, 3.3 mmol) in tetrahydrofuran (5 mL) was added a solution of sodium bis(trimethylsilyl)-amide (3.4 mL, 3.4 mmol), and the resulting mixture was stirred for 1 h at room temperature. The resulting cloudy yellow solution was re-cooled to −30° C., and 1,1-dimethylethyl 4-(4-formyl-2-thiazolyl)-1-piperidinecarboxylate (0.5 g, 1.68 mmol) was added. The resulting slightly yellow solution was stirred at room temperature for 3 h, then diluted with water, and extracted with ethyl acetate. The organic layer was washed with brine, dried (MgSO4), filtered, and purified by column chromatography on silica gel using 15-30% ethyl acetate in hexanes as eluant to give 471 mg of the title compound as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08642634B2
出典データセットuspto-grants-2014_02
ORD IDord-7380437b47cf487f823e37a08c17453c
出典メモuspto-grants-2014_02