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HRID 849997作成日:2026年10月25日

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

https://huagongshe.com/reaction/849997

反応式

関与物質

役割名称HCID仕込み量
反応物O-MethyltyramineHCID 4657—
反応物2-(Bromomethyl)-1,2,3,4-tetrahydronaphthaleneHCID 12723282—
溶媒EthanolHCID 702—
生成物2-[(4-Methoxyphenethyl)aminomethyl]-1,2,3,4-tetrahydronaphthaleneHCID 981764059%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06015819
出典データセットuspto-grants-2000_01
ORD IDord-b5e1d10b546a49858093d42e314a741d
出典メモuspto-grants-2000_01