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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2386898생성일: 2026년 10월 25일

Hydrochloric Acid → 2-(4-Methoxy-2-methylphenyl)-ethylamine hydrochloride

https://huagongshe.com/reaction/2386898

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물2-(4-Methoxy-2-methylphenyl)acetonitrileHCID 3801024—
반응물HCID 178418361HCID 178418361—
촉매PalladiumHCID 23938—
용매EthanolHCID 702—
생성물2-(4-Methoxy-2-methylphenyl)-ethylamine hydrochlorideHCID 6703203450%

반응 단계

4-Methoxy-2-methylphenylacetonitrile (3.0 g, 18.6 mmol) was dissolved in 2B ethanol (65 mL). To the solution was added con. HCl (2.4 mL) and 10% Pd/C (300 mg). The suspension was deaerated in a 500 mL Parr hydrogenation bottle and then pressurized with 55 psi H2, and shaken. After 20 h, the reaction was recharged with hydrogen and 10% Pd/C. After a total of 96 h, the reaction mixture was filtered through Celite and the filtrate was concentrated in vacuo. The off-white solid residue was recrystallized from isopropanol and collected by suction filtration to afford 1.86 g (50% yield) 2-(4-methoxy-2-methylphenyl)-ethylamine hydrochloride as a white solid, melting point (M.P.) 220-222° C. (gradual softening and discoloration from 104-220° C.). The filtrate was concentrated in vacuo and the residue was washed with ethyl acetate and filtered, providing an additional 1.34 g for a total yield of 3.2 g (85% yield). GC/MS: m/z 165; 1H NMR (DMSO) 8.25 (bs, 3H), 7.09 (d, 1H), 6.75 (m, 2H), 3.71 (s, 3H), 2.87 (m, 4H), 2.27 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08268843B2
출처 데이터셋uspto-grants-2012_09
ORD IDord-657fe4badfea4b7ea0caf97763de478f
출처 메모uspto-grants-2012_09