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Acetone → 4-(4-Fluorophenoxy)cyclohexan-1-one

HRID 1723431
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HRID 1723431 반응식
[F:1][C:2]1[CH:15]=[CH:14][C:5]([O:6][CH:7]2[CH2:12][CH2:11][CH:10]([OH:13])[CH2:9][CH2:8]2)=[CH:4][CH:3]=1.CC(=O)C.S(=O)(=O)(O)O.CO>O.[O-2].[O-2].[O-2].[Cr+6]>[F:1][C:2]1[CH:3]=[CH:4][C:5]([O:6][CH:7]2[CH2:8][CH2:9][C:10](=[O:13])[CH2:11][CH2:12]2)=[CH:14][CH:15]=1
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참가 물질

7

반응물 4

HCID 180AcetoneHCID 887MethanolHCID 1118Sulfuric AcidHCID 15725170HCID 15725170, 화합물

생성물 1

HCID 157251714-(4-Fluorophenoxy)cyclohexan-1-one수율 96.1%

시약·촉매·용매 2

HCID 10219390chromium (VI) trioxide촉매
HCID 962
Water
용매

실험 절차

To a stirred and cooled mixture of 8.9 parts of 4-(4-fluorophenoxy)cyclohexanol and 160 parts of 2-propanone were added dropwise 13 parts of a solution of 26.7 parts of chromium trioxide in 42.3 parts of concentrate sulfuric acid diluted with water till a volume of 100 parts at a temperature below 5° C. Upon completion, stirring was continued for 3 hours at room temperature. After the addition of a few parts of methanol, the reaction mixture was poured onto water. The product was extracted with dichloromethane. The extract was dried, filtered and evaporated, yielding 8.4 parts (96.1%) of 4-(4-fluorophenoxy)cyclohexanone as a residue (140).

후처리

  1. temperaturecooled
  2. stirringUpon completion, stirring
  3. additionthe reaction mixture was poured onto water
  4. extractionThe product was extracted with dichloromethane
  5. customThe extract was dried
  6. filtrationfiltered
  7. customevaporated

출처 및 근거

ORD 기록
ord-b81178eb3b7b465a9ff17f79abd8d97f
출처 데이터셋
uspto-grants-1989_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04861785

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