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2,3,4,5,6-Pentafluorobenzophenone → HCID 22481417, 화합물

HRID 1863144
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HRID 1863144 반응식
[F:1][C:2]1[C:7]([C:8]([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)=[O:9])=[C:6]([F:16])[C:5]([F:17])=[C:4]([F:18])[C:3]=1[F:19]>C1C=CC=CC=1.C(O)(C)C>[F:1][C:2]1[C:7]([C:8]([C:8]([C:7]2[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=2)([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[OH:9])([OH:9])[C:10]2[C:15]([F:1])=[C:14]([F:16])[C:13]([F:17])=[C:12]([F:18])[C:11]=2[F:19])=[C:6]([F:16])[C:5]([F:17])=[C:4]([F:18])[C:3]=1[F:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 737552,3,4,5,6-Pentafluorobenzophenone

생성물 1

HCID 22481417HCID 22481417, 화합물

시약·촉매·용매 1

HCID 20154085HCID 20154085, 화합물용매

실험 절차

Pentafluorobenzophenone (10.4 g) was dissolved in 250 ml of benzene/isopropanol (3.5:1). The solution was purged with nitrogen and irradiated for 6 hours with a Hanovia 450-watt Hg-arc lamp. The solvent was removed using a vacuum evaporator at a temperature less than 40° C. The crystallized product was washed twice with 25 ml of n-pentane. The slurry was centrifuged and n-pentane was decanted. The product was spread on a watch glass and air dried. Recovery of 2,3,4,5,6,2',3',4',5',6'-decafluorobenzopinacol was 9.1 g or 87.5%.

후처리

  1. customThe solution was purged with nitrogen
  2. customirradiated for 6 hours with a Hanovia 450-watt Hg-arc lamp
  • customThe solvent was removed
  • customa vacuum evaporator at a temperature less than 40° C
  • washThe crystallized product was washed twice with 25 ml of n-pentane
  • customn-pentane was decanted
  • customdried
  • 출처 및 근거

    ORD 기록
    ord-8fa33a14a54c428d861f2ec3680721d2
    출처 데이터셋
    uspto-grants-1979_09
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04168218

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