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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 614081생성일: 2026년 10월 26일

Furfuryl Alcohol → Pyroxyfur

https://huagongshe.com/reaction/614081

반응식

참여 물질

역할이름HCID투입량
반응물Furfuryl AlcoholHCID 7361—
반응물HexaneHCID 8058—
반응물Sodium hydrideHCID 24758—
반응물2,6-Dichloro-4-(trichloromethyl)pyridineHCID 89782—
용매WaterHCID 962—
용매1,2-DimethoxyethaneHCID 8071—
생성물PyroxyfurHCID 12981358.3%

반응 조건

온도50 °C

반응 단계

To 5.5 grams (0.115 mole) of hexane washed sodium hydride in 100 mls of dimethoxyethane was added over a 25 minute period, 11.28 grams (0.115 mole) of 2-(hydroxymethyl)furan dissolved in 30 mls of dimethoxyethane. An additional 25 mls of dimethoxyethane was added and the mixture heated to 50° C. for about 10 minutes. To this mixture was added 26.54 grams (0.1 mole) of 2,6-dichloro-4-(trichloromethyl)pyridine dissolved in 100 mls of dimethoxyethane. The mixture was heated under reflux (83° C.) for about 2.5 hours and the reaction mixture added to 600 mls of water and extracted with methylene chloride. The methylene chloride was evaporated from the extract leaving a black oil. This oil was distilled under reduced pressure to obtain 19.05 grams of the desired 2-chloro-6-(2-furanylmethoxy)-4-(trichloromethyl)pyridine product. The product, an oil, had a refractive index of n 25/d = 1.5722 and upon analysis was found to have carbon, hydrogen, nitrogen and chlorine contents of 41.19, 2.50, 4.23 and 42.49 percent, respectively, as compared with the theoretical contents of 40.40, 2.16, 4.28 and 43.37 percent, respectively, as calculated for the above named compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04143144
출처 데이터셋uspto-grants-1979_03
ORD IDord-d4e1657eb891471ea47e22abc80d18f7
출처 메모uspto-grants-1979_03