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HRID 84955作成日:2026年10月26日

tert-Butyl acrylate → (E)-tert-Butyl 3-(2-(2-ethoxy-2-oxoethyl)phenyl)acrylate

https://huagongshe.com/reaction/84955

反応式

関与物質

役割名称HCID仕込み量
反応物tert-Butyl acrylateHCID 15458—
反応物Tris(1,1-dimethylethyl)phosphineHCID 83681—
反応物Ethyl 2-(2-bromophenyl)acetateHCID 2780092—
反応物alpha-CyclohexylcyclohexanemethanamineHCID 10774245—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒Ethyl AcetateHCID 8857—
溶媒1,4-DioxaneHCID 31275—
生成物(E)-tert-Butyl 3-(2-(2-ethoxy-2-oxoethyl)phenyl)acrylateHCID 86647801—

反応条件

温度70 °C

反応手順

To a mixture of ethyl 2-(2-bromophenyl)acetate (0.97 g, 4 mmol), t-butyl acrylate (0.51 g, 4 mmol), tris(dibenzylideneacetone)dipalladium(0) (91 mg, 0.1 mmol), dicyclohexylmethylamine (0.98 g, 5 mmol) in dioxane (5 mL) was added tri-tert-butylphosphine (0.2 mL, 1 N in toluene, 0.2 mmol). The mixture was heated at 70° C. for 30 minutes under N2. Ethyl acetate was added, and the mixture was filtered through diatomaceous earth. The filtrate was concentrated and purified by silica gel column chromatography eluting with hexanes and ethyl acetate (10:1) to afford the title compound. 1H NMR (300 MHz, DMSO-d6) δ ppm 7.79 (m, 1H), 7.72 (d, J=15.6 Hz, 1H), 7.34 (m, 3H), 6.40 (d, J=15.7 Hz, 1H), 4.06 (q, J=7.2 Hz, 2H), 3.84 (s, 2H), 1.48 (s, 9H), and 1.17 (t, J=2 Hz, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846951B2
出典データセットuspto-grants-2014_09
ORD IDord-02bb524d6400491e80253008d44c0ca7
出典メモuspto-grants-2014_09