반응 #86674

ord-08902dd1257f4b6f9ee352acd169a027

반응 방정식

ClCC1CO1
epichlorohydrin
Oc1ccc(Oc2ccccc2)cc1
4-phenoxyphenol
OC(CCl)COc1ccc(Oc2ccccc2)cc1
4-phenoxy-O-(2-hydroxy-3-chloropropyl)phenol

시약

없음

용매

반응 조건

온도
70°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타A four-neck flask equipped with a thermometer
  2. 2
    workup.ADDITIONwas added dropwise
  3. 3
    workup.WAITwas performed for 6 hours
  4. 4
    workup.ADDITIONthe addition reaction

실험 절차

A four-neck flask equipped with a thermometer, dropping funnel, condenser tube and stirrer was charged with 305.3 g (3.3 mol) of epichlorohydrin, and while nitrogen purging was performed, the temperature was raised to 70° C. Into the flask, 204.8 g (1.1 mol) of 4-phenoxyphenol dissolved in 1020 g of ethanol was added dropwise taking 4 hours. Further, stirring was performed for 6 hours, to complete the addition reaction, for obtaining 4-phenoxy-O-(2-hydroxy-3-chloropropyl)phenol. In succession, the temperature in the flask was lowered to 25° C., and into the flask, 229 g (2.75 mol) of 48% NaOH aqueous solution was added dropwise taking 2 hours. Further, stirring was performed for 1 hour. After completion of cyclization reaction, ethanol was distilled away, and 410 g of toluene was used for extraction, 5% saline solution being used for washing twice. Toluene and epichlorohydrin were removed from the organic layer under reduced pressure, to obtain 215.6 g of a viscous liquid (yield 89%). The purity of 4-phenoxyphenyl glycidyl ether as the main product was 92% (GCarea %).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09434811B2uspto-grants-2016_09