Ethanol → HCID 68771264、化合物

HRID 1170947

反応式

HRID 1170947 の反応式
[OH:1][C:2]1[CH:3]=[CH:4][C:5]2[C:6](=[O:17])[C:7]3[C:12]([O:13][C:14]=2[CH:15]=1)=[CH:11][C:10]([OH:16])=[CH:9][CH:8]=3.C(O)C.[OH-].[K+].[C:23]([CH2:27][CH2:28][CH2:29][CH2:30][CH2:31]Br)([F:26])([F:25])[F:24]>O>[F:24][C:23]([F:26])([F:25])[CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][O:1][C:2]1[CH:3]=[CH:4][C:5]2[C:6](=[O:17])[C:7]3[C:12]([O:13][C:14]=2[CH:15]=1)=[CH:11][C:10]([OH:16])=[CH:9][CH:8]=3

参加物

6

反応物 4

HCID 702EthanolHCID 14797Potassium Hydroxide2 回HCID 57493223,6-dihydroxy-9H-xanthen-9-oneHCID 138454716-Bromo-1,1,1-trifluorohexane

生成物 1

HCID 68771264HCID 68771264、化合物

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

To 3,6-dihydroxy-xanthone (0.58 g, 1 equivalent) is added 10 ml of ethanol, then 117 mg of KOH 0.8 equivalents), followed by 0.58 g of CF3(CH2)5Br (1 equivalent); after two hours of boiling this mixture, the pH had dropped to the acidic range, and another 100 mg of KOH was added and heating continued overnight. The cooled mixture was diluted with water (50 ml) and extracted with ethyl acetate (3×50 ml), the combined extracts washed with 5 ml of water and brought to dryness. Separation of the 3-component mixture was achieved by chromatography (100 g of silica gel, column diameter 5 cm) with solvents of increasing polarity: Solvents used: ethyl acetate (A), hexane (isomeric mixture) (B), ethanol (C)

後処理

  1. additionthe pH had dropped to the acidic range
  2. temperatureheating continued overnight
  3. extractionextracted with ethyl acetate (3×50 ml)
  4. washthe combined extracts washed with 5 ml of water
  5. customSeparation of the 3-component mixture
  6. temperatureof increasing polarity

出典と根拠

ORDレコード
ord-632095f8161a4f4bb137138c227a7b63
出典データセット
uspto-grants-2010_11
特許番号
US07829578B1

関連ノート

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