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HRID 345996作成日:2026年10月25日

Potassium Carbonate → 2-(1-Acetyl-2,2,6,6-tetramethylpiperidin-4-oxy)-4-(1-hydroxyl-2,2,6,6-tetramethylpiperidin-4-oxy)-6-(2,2,6,6-tetramethylpiperidin-1-yl)-1,3,5-triazine

https://huagongshe.com/reaction/345996

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物Potassium HydroxideHCID 14797—
反応物1-(4-Hydroxy-2,2,6,6-tetramethylpiperidin-1-yl)ethan-1-oneHCID 14549312—
反応物2-Chloro-4-(1-hydroxyl-2,2,6,6-tetramethylpiperidin-4-oxy)-6-(2,2,6,6-tetramethylpiperidin-1-yl)-1,3,5-triazineHCID 19991796—
触媒Tetrabutylammonium hydrogen sulfateHCID 94433—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物2-(1-Acetyl-2,2,6,6-tetramethylpiperidin-4-oxy)-4-(1-hydroxyl-2,2,6,6-tetramethylpiperidin-4-oxy)-6-(2,2,6,6-tetramethylpiperidin-1-yl)-1,3,5-triazineHCID 19991782—

反応手順

4 g of 2-chloro-4-(1-hydroxyl-2,2,6,6-tetramethylpiperidin-4-oxy)-6-(2,2,6,6-tetramethylpiperidin-1-yl)-1,3,5-triazine (product from Example 36) are dissolved in 30 ml of toluene, after which 2.6 g of pulverized KOH, 1 g of potassium carbonate and 0.15 g of tetrabutylammonium hydrogen sulfate are added. 1.95 g of 1-acetyl-2,2,6,6-tetramethyl-4-hydroxypiperidine are added with stirring. The mixture is warmed to 60° for 17 hours. After cooling, 30 ml of water are added. The phases are separated. The organic phase is dried over Na2SO4 and evaporated. After recrystalling from methylene chloride/hexane, dissolving the product in hexane/acetic acid and chromatographic purification on an SiO2 column, the above product, which melts at 175°-176°, is obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05059689
出典データセットuspto-grants-1991_10
ORD IDord-2de703f90ef243378d4f1d60e919c3a2
出典メモuspto-grants-1991_10