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HRID 133645作成日:2026年10月26日

Hydrogen Peroxide → 1-Cyclohexyloxy-4-benzoyloxy-2,2,6,6-tetramethylpiperidine

https://huagongshe.com/reaction/133645

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrogen PeroxideHCID 784—
反応物AcetonitrileHCID 6342—
反応物Boric AcidHCID 7628—
反応物1-Hydroxy-4-benzoyloxy-2,2,6,6-tetramethylpiperidineHCID 688178—
触媒Boric AcidHCID 7628—
溶媒WaterHCID 962—
溶媒CyclohexaneHCID 8078—
生成物1-Cyclohexyloxy-4-benzoyloxy-2,2,6,6-tetramethylpiperidineHCID 2337209868%

反応条件

温度52 °C

反応手順

A solution of 0.100 g (0.360 mmol) of ferrous sulfate heptahydrate and 0.112 g (1.82 mmol) of boric acid in 4 ml of water is added to a mixture of 5.00 g (18.1 mmol) of 1-oxyl-4-benzoyloxy-2,2,6,6-tetramethylpiperidine, 27 ml of acetonitrile, and 19 ml of cyclohexane. The mixture is heated to 52° C. A solution of 4.98 g (73 mmol) of 50% aqueous hydrogen peroxide is added dropwise over 2.75 hours to the reaction mixture while the temperature is brought to and maintained at reflux (63° C.). A solution of 0.051 g of ferrous sulfate heptahydrate and 0.042 g of boric acid in 2 ml of water is added to the reaction mixture 1.25 hours after the peroxide addition is started. After the peroxide is added, the reaction mixture is heated at reflux for 30 minutes, then allowed to cool slowly. Work-up and purification according to the procedure of Example 5 afford 4.42 g (68% yield) of the title compound, a colorless syrup, GC assay 99.3%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07390904B2
出典データセットuspto-grants-2008_06
ORD IDord-3be2a870370043d3af12d94d8a753174
出典メモuspto-grants-2008_06