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HRID 322804作成日:2026年10月24日

1,4-Dihydroxy-2,2,6,6-tetramethylpiperidine → 1-(Cycloocta-2,6-dienyloxy)-2,2,6,6-tetramethyl-4-hydroxypiperidine

https://huagongshe.com/ja/reaction/322804

反応式

関与物質

役割名称HCID仕込み量
反応物1,4-Dihydroxy-2,2,6,6-tetramethylpiperidineHCID 5395—
反応物cis,cis-1,5-CyclooctadieneHCID 8135—
生成物1-(Cycloocta-2,6-dienyloxy)-2,2,6,6-tetramethyl-4-hydroxypiperidineHCID 7024052033%

反応条件

温度100 °C

反応手順

A mixture of 29.4 g (0.17 mol) of 1-oxyl-4-hydroxy-2,2,6,6-tetramethylpiperidine and 148.0 g (1.37 mol) of 1,5-cyclooctadiene is heated under a nitrogen atmosphere at 100° C. for 24 hours. The reaction mixture is filtered to remove 1,4-dihydroxy-2,2,6,6-tetramethylpiperidine, and the filtrate is diluted with heptane (250 mL). The organic phase is washed with 5% ascorbic acid (2×50 mL) and distilled water (2×50 mL). The organic phase is dried over anhydrous magnesium sulfate and the volatiles removed in vacuo. The residue is chromatographed to give 8.1 g (33% yield) of the title compound as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06211378B1
出典データセットuspto-grants-2001_04
ORD IDord-72a4d00cc3ca48cf9cad41f1c627458b
出典メモuspto-grants-2001_04