돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 462424생성일: 2026년 10월 26일

Furan → 3-Chloro-1-(2-furanyl)-1-propanone

https://huagongshe.com/reaction/462424

반응식

참여 물질

역할이름HCID투입량
반응물FuranHCID 8029—
반응물3-Chloropropionyl chlorideHCID 69364—
반응물Aluminum(III) ChlorideHCID 6451240—
용매1,2-DichloroethaneHCID 11—
생성물3-Chloro-1-(2-furanyl)-1-propanoneHCID 2039829511%

반응 단계

At 25°, 3-chloropropionyl chloride (25.4 g, 0.20 mole) was added to a suspension of anhydrous aluminum chloride (27.1 g, 0.20 mole) in 1,2-dichloroethane (DCE). The mixture was stirred until the aluminum chloride had nearly dissolved. This solution was added at 0°-5° during 15 minutes to a solution of furan (13.6 g, 0.2 mole) in 100 ml of DCE. The reaction mixture became very dark and a tan precipitate was deposited. The reaction mixture was then immediately poured into 1 of ice-water. An emulsion of some brown precipitate formed. This mixture was extracted with diethyl ether (five times, 150 ml), and the combined ether extract was filtered through a column of 150 g of silica gel. The column was then washed with 200 ml of ether and the combined eluants were concentrated at reduced pressure (40°) to 100 ml. The solution was then washed with 100 ml of saturated sodium hydrogen carbonate, dried over anhydrous sodium sulfate, treated with activated carbon, and evaporated at reduced pressure to give a liquid (3.5 g) which rapidly darkened at room temperature. It was stored at -10°. PMR spectroscopy indicated the product was about 75% desired copound. The mixture was used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04515793
출처 데이터셋uspto-grants-1985_05
ORD IDord-a9a33b99cc174818991b83062c287a2f
출처 메모uspto-grants-1985_05