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HRID 130707作成日:2026年10月26日

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

https://huagongshe.com/reaction/130707

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US07381719B2
出典データセットuspto-grants-2008_06
ORD IDord-ccf243a42fc24f19b931160a3d67fead
出典メモuspto-grants-2008_06