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HRID 127728作成日:2026年10月27日

4-Benzhydrylpiperidine → HCID 12796197、化合物

https://huagongshe.com/reaction/127728

反応式

関与物質

役割名称HCID仕込み量
反応物4-BenzhydrylpiperidineHCID 88278—
反応物6-(3,5-Dioxomorpholino)hexyl p-toluenesulfonateHCID 12796194—
溶媒tert-ButanolHCID 6386—
生成物HCID 12796197HCID 12796197149.6%

反応手順

To a solution of 9.75 grams (26.39 millimoles) of 6-(3,5-dioxomorpholino)hexyl p-toluenesulfonate (prepared as described in Example IX) in 160 milliliters of warm tertiary butyl alcohol was added portionwise at temperatures in the range of 30°-32° C. over a period of about 23 minutes, 63 grams (26.38 millimoles) of 4-benzhydrylpiperidine in 160 milliliters of tertiary-butyl alcohol. The reaction mixture was heated at reflux temperature for about 22 hours and thereafter the solvent removed by vaporization to obtain 17.7 grams of a 4-[6-(4-benzhydrylpiperidino)hexyl]-3,5-dioxomorpholine product as a yellow oil. Crystallization (twice) from ethyl acetate produced 4.19 grams of white crystals, m.p., 121°-124.5° C. and having NMR, UV and IR spectral characteristics appropriate for the product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04256891
出典データセットuspto-grants-1981_03
ORD IDord-555f25c28eb04998b04b819d870496e5
出典メモuspto-grants-1981_03