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HRID 216133作成日:2026年10月26日

Methyl iodide → 2-(4-Methoxyphenyl)-2-methylpropan-1-amine

https://huagongshe.com/reaction/216133

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物CyclohexaneHCID 8078—
反応物Benzeneacetonitrile, 4-methoxy-HCID 66031—
反応物2-(4-Methoxyphenyl)-2-methylpropanenitrileHCID 219166—
反応物Lithium diisopropylamideHCID 2724682—
反応物2-(4-Ethoxyphenyl)propanenitrileHCID 13254522—
反応物Aluminium lithium hydrideHCID 21226445—
溶媒TetrahydrofuranHCID 8028—
溶媒Ammonium ChlorideHCID 25517—
生成物2-(4-Methoxyphenyl)-2-methylpropan-1-amineHCID 358136433%

反応手順

To a solution of (4-methoxy-phenyl)-acetonitrile [5 g, 34 mmol] in THF (40 mL), is added a 1.5 M solution of lithium diisopropylamide in cyclohexane (36 mL, 54 mmol) at −78° C. After 2 hours at −78° C., methyl iodide (3.4 g, 54 mmol) is added, and the mixture is allowed to warm to room temperature over 3 hours. After additional 12 hours at 20° C., the mixture is diluted with aqueous ammonium chloride solution, and extracted with ethyl acetate. The extracts are dried over magnesium sulfate, filtered and concentrated. The residue is subjected to chromatography on silica gel eluting with 40% EtOAc in heptane to afford a mixture of 2-(4-ethoxy-phenyl)-propionitrile and 2-(4-methoxy-phenyl)-2-methyl-propionitrile. To above mixture (5 g) in THF (20 mL) is add a 2 M solution of lithium aluminum hydride (35 mL, 70 mmol) at 0° C. After 12 hours at 20° C., the mixture is carefully quenched with 10% sodium hydroxide solution, and the white slurry is diluted with ether. The mixture is dried over magnesium sulfate, filtered and concentrated. The residue is subjected to chromatography on silica to afford 2-(4-methoxy-phenyl)-2-methyl-propylamine [2 g, 33%, Intermediate (35)]. MS: 180 (M+H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08193183B2
出典データセットuspto-grants-2012_06
ORD IDord-a2e8851f2c1d4f27b7ceaa176f8c7208
出典メモuspto-grants-2012_06