戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 64129作成日:2026年10月24日

Nitrogen → N-(3-(benzofuran-2-yl)-5-nitrophenyl)acetamide

https://huagongshe.com/ja/reaction/64129

反応式

関与物質

役割名称HCID仕込み量
反応物NitrogenHCID 947—
反応物Sodium CarbonateHCID 10340—
反応物N-(3-bromo-5-nitrophenyl)acetamideHCID 10658908—
反応物2-(1-Benzofuran-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 11368533—
触媒Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物N-(3-(benzofuran-2-yl)-5-nitrophenyl)acetamideHCID 89500178—

反応手順

A solution of N-(3-bromo-5-nitrophenyl)acetamide of Example 1(c) (2 g, 7.7 mmol) in 1,2-dimethoxyethane (25 ml) was degassed by N2 bubbling for 5 min. 2-(Benzofuran-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (2.45 g, 10 mmol, 1.3 eq.) was added and the mixture was degassed for another 5 min. Pd(dppf)Cl2 (0.63 g, 0.77 mmol, 0.1 eq.) and aqueous sodium carbonate (2.45 g, 23.1 mmol, 3.0 eq.) were added and the procedure of Example 1(d) was followed. The crude residue of the product was directly used for the next step.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09447091B2
出典データセットuspto-grants-2016_09
ORD IDord-1e27b309856a4d778203c36fa0fb4ba4
出典メモuspto-grants-2016_09