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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1535039생성일: 2026년 10월 26일

Carbon Tetrachloride → 1,3,5-Trichloro-2-(2-chloroethoxy)benzene

https://huagongshe.com/reaction/1535039

반응식

참여 물질

역할이름HCID투입량
반응물Carbon TetrachlorideHCID 5943—
반응물Thionyl ChlorideHCID 24386—
반응물2-(2,4,6-Trichlorophenoxy)ethan-1-olHCID 96343—
촉매Benzyltrimethylammonium chlorideHCID 5963—
용매WaterHCID 962—
생성물1,3,5-Trichloro-2-(2-chloroethoxy)benzeneHCID 1127695998%

반응 조건

온도55 °C

반응 단계

Into a three-necked, round-bottom flask fitted with a stirrer, thermometer, reflux condenser and dropping funnel was added 250 g of 96% 2-(2,4,6-trichlorophenoxy) ethanol, 250 ml carbon tetrachloride and 4 g of benzyl-trimethyl-ammonium chloride. The mixture was heated to 55° C. and 146 g thionyl chloride was added dropwise over 1.5 hours. After the addition of the thionyl chloride the temperature of the reaction was slowly raised to 80° C. for a total reaction tme of 2.5 to 3 hours. The end of the reaction was determined by GLC. The mixture was cooled to 60° C. and water slowly added to decompose the excess thionyl chloride. The phases were separated and the organic phase was washed with a 10% sodium hydroxide solution until it reached a pH of 7. After an additional separation of the phases the organic phase was washed again with water. After a further separation of phases, the carbon tetrachloride was distilled off to yield an oil which slowly crystallized to form 257 g of 2-(2,4,6-trichlorophenoxy)-ethyl chloride in a purity of 96%-98% and yield of 98%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05091578
출처 데이터셋uspto-grants-1992_02
ORD IDord-83e99dc639134bbfa83ebdc2cc54716a
출처 메모uspto-grants-1992_02