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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 65891생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/65891

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Diethyl EtherHCID 3283—
반응물2,4-DihydroxybenzophenoneHCID 8572—
반응물4-[(E)-tert-Butyldiazenyl]-4-cyanopentanoyl chlorideHCID 15274024—
용매WaterHCID 962—
생성물4-(4-t-Butylazo-4-cyanovaleryloxy)-2-hydroxybenzophenoneHCID 2056347399%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04129586
출처 데이터셋uspto-grants-1978_12
ORD IDord-2c38ccc94d1546ba92a2bed4bc5bdd04
출처 메모uspto-grants-1978_12