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HRID 65891作成日:2026年10月26日

Pyridine → 4-(4-t-Butylazo-4-cyanovaleryloxy)-2-hydroxybenzophenone

https://huagongshe.com/reaction/65891

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Diethyl EtherHCID 3283—
反応物2,4-DihydroxybenzophenoneHCID 8572—
反応物4-[(E)-tert-Butyldiazenyl]-4-cyanopentanoyl chlorideHCID 15274024—
溶媒WaterHCID 962—
生成物4-(4-t-Butylazo-4-cyanovaleryloxy)-2-hydroxybenzophenoneHCID 2056347399%

反応手順

To a solution of 4.7 g. (0.022 m) of 2,4-dihydroxybenzophenone and 2.5 ml. of pyridine in 35 ml. of ether in a 4 neck 100 ml. round bottom flask containing a thermometer, condenser and magnetic stirring bar was added 4.0 g. (0.0218 m) of 4-t-butylazo-4-cyanovaleryl chloride dropwise with cooling so the temperature did not rise above 25° C. After completion of the addition the reaction mixture was stirred 1/2 hour at room temperature and then diluted with 100 ml. of water. The ether layer was separated, washed consecutively with 5% HCl, water, and 10% NaHCO3 solution and saturated sodium chloride solution. The ether was evaporated off and the residue dissolved in methylene chloride, dried over anhydrous sodium sulfate, filtered and the methylene chloride stripped off under reduced pressure. The product weighted 8.8 g. (99% yield) and was a viscous syrup. The infrared spectrum was in agreement with the structure of the desired product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04129586
出典データセットuspto-grants-1978_12
ORD IDord-2c38ccc94d1546ba92a2bed4bc5bdd04
出典メモuspto-grants-1978_12