戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 243705作成日:2026年10月27日

Tributylstannane → Benzyl 2-(tributylstannyl)acrylate

https://huagongshe.com/reaction/243705

反応式

関与物質

役割名称HCID仕込み量
反応物TributylstannaneHCID 5948—
反応物Benzyl propiolateHCID 543064—
触媒HCID 178418397HCID 178418397—
溶媒TetrahydrofuranHCID 8028—
生成物Benzyl 2-(tributylstannyl)acrylateHCID 6683874173%

反応手順

To a solution of 6.42 g (40.1 mmol) of benzyl propiolate from step A above in 25 ml of anhydrous THF was added 0.93 g (0.80 mmol) of tetrakis(triphenylphosphine)palladium(0) followed by a solution of 12.6 g (42.1 mmol) of tributyltin hydride in 25 mL of anhydrous THF over 15 min. After stirring at room temperature overnight the solvent was removed under reduced pressure. The residue was filtered through a pad of Celite® which was then washed with hexanes. The filtrate was concentrated in vacuo and the crude product was purified by silica gel chromatography eluting with a 0-15% ethyl acetate in hexane gradient to afford the title compound as a colorless oil (13 g, 73%). 1H NMR (CDCl3, 500 MHz) δ 7.39 (m, 5H), 6.99 (d, J=2.7 Hz, 1H), 5.98 (d, J=2.7 Hz, 1H), 5.20 (s, 2H), 1.47 (m, 6H), 1.30 (m, 6H), 0.96 (m, 6H), 0.89 (t, J=7.4 Hz, 9H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08653260B2
出典データセットuspto-grants-2014_02
ORD IDord-af0cb9cd4c6341da8df5d6a3413ad6c1
出典メモuspto-grants-2014_02