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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2117523생성일: 2026년 10월 26일

Ammonium Hydroxide → 3-(3-Aminomethyl-phenyl)-2-methyl-propionic acid methyl ester

https://huagongshe.com/reaction/2117523

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium HydroxideHCID 14923—
반응물3-(3-Cyano-phenyl)-2-methyl-propionic acid methyl esterHCID 54523024—
촉매PalladiumHCID 23938—
용매MethanolHCID 887—
용매Ethyl AcetateHCID 8857—
생성물Ammonium HydroxideHCID 14923—
생성물3-(3-Aminomethyl-phenyl)-2-methyl-propionic acid methyl esterHCID 53702591144.7%

반응 단계

A mixture of 3-(3-cyano-phenyl)-2-methyl-propionic acid methyl ester of Step B (62 mg, 0.30 mmol) and palladium on carbon (10%, 50 mg) in MeOH (10 mL), EtOAc (10 mL), and ammonium hydroxide (5 mL) was hydrogenated at 40 psi for 24 h. The catalyst was removed via filtration through Celite with the aid of MeOH. The solvent was removed in vacuo. Chromatography (1:1 hexanes:EtOAc to CH2Cl2:MeOH:NH4OH, 95:5:0.1) provided the title compound of Step C (45 mg). 1H NMR (400 MHz, CD3OD) δ 7.31-7.14 (m, 4H), 3.94 (s, 2H), 3.59 (s, 3H), 2.96 (m, 1H), 2.72 (m, 2H), 1.12 (d, 3H); MS 208 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07442702B2
출처 데이터셋uspto-grants-2008_10
ORD IDord-120b5c5a44184a788669a7139fadc03c
출처 메모uspto-grants-2008_10