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HRID 126796作成日:2026年10月26日

5H-(1)Benzopyrano(4,3-c)pyridine, 1,2,3,4-tetrahydro-5,5-dimethyl-8-(1,2-dimethylheptyl)-10-hydroxy- → 5,5-Dimethyl-10-hydroxy-8-(3-methyl-2-octyl)-5H-[1]benzopyrano[3,4-d]pyridine

https://huagongshe.com/reaction/126796

反応式

関与物質

役割名称HCID仕込み量
反応物5H-(1)Benzopyrano(4,3-c)pyridine, 1,2,3,4-tetrahydro-5,5-dimethyl-8-(1,2-dimethylheptyl)-10-hydroxy-HCID 213543—
触媒PalladiumHCID 23938—
溶媒O-XyleneHCID 7237—
生成物5,5-Dimethyl-10-hydroxy-8-(3-methyl-2-octyl)-5H-[1]benzopyrano[3,4-d]pyridineHCID 19781402—

反応手順

A mixture of 4.20 g. of 5,5-dimethyl-10-hydroxy-8-(3-methyl-2-octyl)-1,2,3,4-tetrahydro-5H-[1]benzopyrano[3,4-d]pyridine, 0.8 g. of 10% palladium on carbon and 80 ml. of xylene was stirred and refluxed for 25 hours. After cooling, the catalyst was removed by filtration. The filtrate was evaporated in vacuo and the product was recrystallized from autonitrile; m.p. 155°-157°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04254116
出典データセットuspto-grants-1981_03
ORD IDord-62e66fd39837453fa9f80da2252cafb7
出典メモuspto-grants-1981_03