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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 394566생성일: 2026년 10월 25일

O-Methyltyramine → 2-[(4-Methoxyphenethyl)aminomethyl]-1,2,3,4-tetrahydronaphthalene

https://huagongshe.com/reaction/394566

반응식

참여 물질

역할이름HCID투입량
반응물O-MethyltyramineHCID 4657—
반응물2-(Bromomethyl)-1,2,3,4-tetrahydronaphthaleneHCID 12723282—
용매EthanolHCID 702—
생성물2-[(4-Methoxyphenethyl)aminomethyl]-1,2,3,4-tetrahydronaphthaleneHCID 981764059%

반응 단계

A solution of 2-bromomethyl-1,2,3,4-tetrahydronaphthalene (1.33 g, 5.91 mmol) and 4-methoxyphenethylamine (1.79 g, 11.8 mmol) in 50 ml of EtOH was refluxed for 48 hours. After removal of EtOH in vacuo, the residue was dissolved in 100 ml of CHCl3, washed with 10% K2CO3, H2O, sat'd brine, and then dried over Na2SO4. Filtration followed by evaporation of solvent gave a yellow oil, which was purified by chromatography (SiO2, MeOH:CHCl3, 5:95) to a give a yellowish oil (1.03 g, 58.9%). The product was converted to HCl salt, crystallization with MeOH/Et2O gave a white powder. mp 274-275° C.; Calcd for C20H25NO.HCl: C 72.37, H 7.91, N 4.22; Found C 72.40, H 7.76, N 4.13.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06602888B2
출처 데이터셋uspto-grants-2003_08
ORD IDord-fd6b8ab93ae64f53a5c3385916bd08bf
출처 메모uspto-grants-2003_08