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HRID 1296849作成日:2026年10月24日

rel-(2R,6S)-2,6-Dimethylpiperidine → 1-(2-(2,6-Dimethylpiperidyl)ethoxy)-4-((4-chloronaphthyloxy)methyl)benzene

https://huagongshe.com/ja/reaction/1296849

反応式

関与物質

役割名称HCID仕込み量
反応物rel-(2R,6S)-2,6-DimethylpiperidineHCID 641768—
反応物2-Chloro-1-(4-((4-chloronaphthyloxy)methyl)phenoxy)ethaneHCID 23514395—
生成物1-(2-(2,6-Dimethylpiperidyl)ethoxy)-4-((4-chloronaphthyloxy)methyl)benzeneHCID 2351440947.2%

反応手順

A stirred mixture of 0.4 grams (0.001 mole) of 2-chloro-1-(4-((4-chloronaphthyloxy)methyl)phenoxy)ethane and 5 mL (0.037 mole) of cis-2,6-dimethylpiperidine was heated to just below reflux for about 72 hours. After this time, the reaction mixture was analyzed by thin layer chromatography (TLC), which indicated the reaction was incomplete. The reaction mixture was concentrated under reduced pressure and subject to column chromatography on silica gel, yielding 0.2 gram of compound 106. The NMR spectrum was consistent with the proposed structure.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07247756B2
出典データセットuspto-grants-2007_07
ORD IDord-01e21882f70e44d7ad4b31fa479f4c53
出典メモuspto-grants-2007_07