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HRID 228164作成日:2026年10月27日

Hydrochloric Acid → 2-(4-Methoxyphenyl)-2-methylpropanenitrile

https://huagongshe.com/reaction/228164

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物IsobutyronitrileHCID 6559—
反応物4-FluoroanisoleHCID 9987—
反応物Potassium bis(trimethylsilyl)amideHCID 3251421—
溶媒TetrahydrofuranHCID 8028—
生成物2-(4-Methoxyphenyl)-2-methylpropanenitrileHCID 21916652%

反応手順

Add potassium bis(trimethylsilyl)amide (39.90 g, 200 mmol) to a stirred solution of 4-fluoroanisole (15.0 mL, 133 mmol), isobutyronitrile (49.0 mL, 539 mmol) and anhydrous tetrahydrofuran (150 mL). Heat the reaction to reflux under nitrogen for 72 h. Cool the reaction to room temperature, pour it into 1 N hydrochloric acid (300 mL), and extract with diethyl ether (3×100 mL). Wash the diethyl ether extracts with brine (100 mL), dry the extracts over magnesium sulfate, filter, and concentrate on a rotary evaporator to give the crude product. The crude product is purified by flash chromatography on silica gel eluting with 10% ethyl acetate/hexanes to yield 12.13 g (52%) of 2-(4-methoxy-phenyl)-2-methyl-propionitrile: TLC: Rf in 10% ethyl acetate/hexanes: 0.30; 1H NMR (CDCl3): 7.40-7.37 (m, 2H), 6.92-6.90 (m, 2H), 3.81 (s, 3H), 1.70 (s, 6H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07560463B2
出典データセットuspto-grants-2009_07
ORD IDord-f3dcd6e3ee9947f6902923fb0c4cec45
出典メモuspto-grants-2009_07