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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 216133생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/216133

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물CyclohexaneHCID 8078—
반응물Benzeneacetonitrile, 4-methoxy-HCID 66031—
반응물2-(4-Methoxyphenyl)-2-methylpropanenitrileHCID 219166—
반응물Lithium diisopropylamideHCID 2724682—
반응물2-(4-Ethoxyphenyl)propanenitrileHCID 13254522—
반응물Aluminium lithium hydrideHCID 21226445—
용매TetrahydrofuranHCID 8028—
용매Ammonium ChlorideHCID 25517—
생성물2-(4-Methoxyphenyl)-2-methylpropan-1-amineHCID 358136433%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08193183B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-a2e8851f2c1d4f27b7ceaa176f8c7208
출처 메모uspto-grants-2012_06