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HRID 5280作成日:2026年10月23日

Sodium Hydroxide → 2-(4-Decyloxyphenyl)-5-carboxybenzooxazole

https://huagongshe.com/ja/reaction/5280

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物Chloric acidHCID 19654—
反応物Bromic acidHCID 24445—
反応物2-(4-Decyloxyphenyl)-5-acetylbenzoxazoleHCID 19021153—
反応物Sodium hypobromiteHCID 23673712—
溶媒WaterHCID 962—
溶媒1,4-DioxaneHCID 31275—
生成物2-(4-Decyloxyphenyl)-5-carboxybenzooxazoleHCID 1979540975%

反応条件

温度-6.25 °C

反応手順

Example Compound I-51 was synthesized through the following steps: ##STR88## 1.61 g (40.3 m mole) of sodium hydroxide was dissolved in 10.7 ml of water, followed by cooling at -7.5--5° C. on ice-common salt bath. To the solution, 0.66 ml (25.6 m mole) of bromic acid was added dropwise under stirring, followed by cooling at ca. -5° C. To the mixture solution, 4.2 ml of dioxane was added dropwise under stirring to prepare sodium hypobromite solution. In a 200 ml three-neck flask, 1.50 g (3.81 m mole) of (4-decyloxyphenyl)-5-acetylbenzooxazole synthesized in Example 3, 30 ml of dioxane and 2.5 ml of water were placed, followed by keeping inner temperature below 5° C. under cooling with ice and stirring. To the mixture solution, the above-mentioned sodium hypobromite solution was added dropwise, and the reaction temperature was raised up to 45° C. and maintained for 90 minutes. After the reaction, the reaction mixture was poured into 150 ml of water. To the resultant reaction mixture, 3.2 ml of chloric acid was added to show pH=1 to precipitate a crystal. The crystal was filtered and washed with water, followed by recrystallizing from a mixture solvent of acetone-methanol to obtain 1.13 g of 2-(4-decyloxyphenyl)-5-carboxybenzooxazole (Yield: 75.0%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05244596
出典データセットuspto-grants-1993_09
ORD IDord-07d0a3d4d786447dba463b8c0927c013
出典メモuspto-grants-1993_09