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

HRID 1085681
ノート
印刷プレビュー

反応式

HRID 1085681 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 180AcetoneHCID 887MethanolHCID 1118Sulfuric AcidHCID 15725170HCID 15725170、化合物

生成物 1

HCID 157251714-(4-Fluorophenoxy)cyclohexan-1-one収率 96.1%

試薬・触媒・溶媒 2

HCID 10219390chromium (VI) trioxide触媒
HCID 962
Water
溶媒

実験手順

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).

後処理

  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

出典と根拠

ORDレコード
ord-bc68d69b61b94f7296f5af3d00c3911c
出典データセット
uspto-grants-1991_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05010198

反応ノート

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