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HRID 471668作成日:2026年10月25日

Ammonium Hydroxide → 2-Amino-6-(4,5-dihydrofuran-2-yl)benzonitrile

https://huagongshe.com/reaction/471668

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium HydroxideHCID 14923—
反応物Ammonium ChlorideHCID 25517—
反応物2-Amino-6-bromobenzonitrileHCID 9813038—
反応物(4,5-Dihydrofuran-2-yl)trimethylstannaneHCID 10243055—
触媒Tetrakis(triphenylphosphine)palladiumHCID 11979704—
溶媒TolueneHCID 1140—
生成物2-Amino-6-(4,5-dihydrofuran-2-yl)benzonitrileHCID 6674613268%

反応手順

2-Amino-6-bromobenzonitrile (0.75 g, 3.81 mmol), (4,5-dihydrofuran-2-yl)trimethylstannane (Menez, P.; Fargeas, V.; Poisson, J.; Ardisson, J.; Lallemand, J.-Y.; Pancrazi, A. Tetrahedron Letters 1994, 35(42), 7767) (1.02 g, 4.38 mmol), and palladium tetrakis(triphenylphosphine) (0.33 g, 0.28 mmol) were refluxed in toluene (10.0 mL) under nitrogen for 1.5 h. Saturated ammonium chloride (12 mL) and ammonium hydroxide (4 mL) were added, and the mixture was extracted with EtOAc. The organic layer was concentrated under vacuum and the residue was purified by chromatography on silica using 35% EtOAc/hexanes to give 0.48 g (68%) of the title compound as yellow oil. 1H NMR (400 MHz, Acetone-d6) δ 2.78-2.83 (m, 2H), 4.40 (t, J=9.2 Hz, 2H), 5.76 (t, J=3.2 Hz, 1H), 6.04 (s, 2H), 6.77-6.80 (m, 2H), 7.28 (t, J=8.0 Hz, 1H). MS 187 (MH+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08633186B2
出典データセットuspto-grants-2014_01
ORD IDord-7b08581b4034451f9de06ddc8a4964a4
出典メモuspto-grants-2014_01