戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 515757作成日:2026年10月26日

Tributylamine → (E)-tert-butyl 3-(2-acetyl-5-chlorophenyl)acrylate

https://huagongshe.com/reaction/515757

反応式

関与物質

役割名称HCID仕込み量
反応物TributylamineHCID 7622—
反応物tert-Butyl acrylateHCID 15458—
反応物1-(2-Bromo-4-chlorophenyl)ethanoneHCID 4712644—
触媒PalladiumHCID 23938—
触媒palladium(II) acetateHCID 167845—
溶媒DimethylformamideHCID 6228—
生成物(E)-tert-butyl 3-(2-acetyl-5-chlorophenyl)acrylateHCID 8949988363.2%

反応条件

温度100 °C

反応手順

To a degassed solution of 1-(2-bromo-4-chlorophenyl)ethanone (1.0 g, 4.28 mmol), tributylamine (2.041 mL, 8.57 mmol), and tert-butyl acrylate (1.255 mL, 8.57 mmol) in DMF (10 mL) was added palladium on carbon (0.456 g, 0.428 mmol) and Pd(OAc)2 (0.096 g, 0.428 mmol). The reaction mixture was warmed to 100° C. After 16 h, the reaction was cooled to rt. The reaction was filtered and the solid was rinsed with DMF. The filtrate was diluted with EtOAc, washed with H2O (2×), brine, dried over Na2SO4, filtered and concentrated. Purification by normal phase chromatography afforded Intermediate 4A (0.760 g, 63%), as a brown oil. MS (ESI) m/z: 225.0 (M-C4H8+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09108951B2
出典データセットuspto-grants-2015_08
ORD IDord-e6109ceab95f42b99835a4e040a87c59
出典メモuspto-grants-2015_08