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HRID 322593생성일: 2026년 10월 25일

2-Chloroacetophenone → N-[3-methyl-3-(2-chlorophenyl)propyl]-1-(3-methoxyphenyl)ethylamine

https://huagongshe.com/reaction/322593

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참여 물질

역할이름HCID투입량
반응물2-ChloroacetophenoneHCID 10757—
반응물3-MethoxyacetophenoneHCID 11460—
반응물DeuteriumHCID 24523—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물3-(2-Chlorophenyl)butan-1-amineHCID 22011075—
반응물3-Methyl-3-(2-chlorophenyl)cinnamonitrileHCID 69709971—
촉매Titanium isopropoxideHCID 11026—
촉매Palladium hydroxideHCID 9942167—
용매Acetic AcidHCID 176—
생성물N-[3-methyl-3-(2-chlorophenyl)propyl]-1-(3-methoxyphenyl)ethylamineHCID 22011056—

반응 단계

In a similar fashion, 2-chloroacetophenone was used to prepare 3-methyl-3-(2-chlorophenyl)cinnamonitrile. The nitrile was catalytically reduced (palladium hydroxide, acetic acid, 60 p.s.i. hydrogen 2 hr) to generate 3-methyl-3-(2-chlorophenyl)propylamine. An equal molar amount of the amine, 3′-methoxyacetophenone and 1.25 molar equivalents titanium(IV) isopropoxide were mixed 4 hr at rt and the intermediate imine treated with an ethanolic sodium cyanoborohydride (5 ml of 1 M, 5 mmol). Work-up and chromatography afforded N-[3-methyl-3-(2-chlorophenyl)propyl]-1-(3-methoxyphenyl)ethylamine, 4Y, as an oil; m/z (rel. int.) 283 (M+, 17), 268 (71), 164 (13), 135 (100), 121 (21), 105 (27), 91 (26), 77 (14).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06211244B1
출처 데이터셋uspto-grants-2001_04
ORD IDord-b790e942ceba4fab839c4257a694ce62
출처 메모uspto-grants-2001_04