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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Water → HCID 21252689、化合物

HRID 1530800
ノート
印刷プレビュー

反応式

HRID 1530800 の反応式
[F:1][C:2]([F:13])([F:12])[CH2:3][CH2:4][CH:5]1[CH2:10][CH2:9][CH:8]([OH:11])[CH2:7][CH2:6]1.O.CC(C)=O.OS(O)(=O)=O.O=[Cr](=O)=O.C(=O)([O-])O.[Na+]>CC(C)=O.C(O)(C)C>[F:1][C:2]([F:12])([F:13])[CH2:3][CH2:4][CH:5]1[CH2:10][CH2:9][C:8](=[O:11])[CH2:7][CH2:6]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 962WaterHCID 516892Sodium BicarbonateHCID 21252690HCID 21252690、化合物HCID 131709961Jones' reagent

生成物 1

HCID 21252689HCID 21252689、化合物

試薬・触媒・溶媒 2

HCID 180Acetone溶媒HCID 3776
Isopropanol
溶媒

実験手順

35.6 g of 4-(3,3,3-trifluoropropyl)cyclohexanol were dissolved in 600 ml of acetone and 37 ml of water and mixed with 69 ml of Jones reagent. The mixture was stirred at room temperature for 24 h, mixed with 9 ml of isopropanol and 24 g of sodium hydrogen carbonate, the precipitate was filtered off and the residue was taken up in saturated aqueous sodium chloride. The mixture was extracted with ether and the combined ether phases were washed with water, dried and concentrated. Chromatography over silica gel (petroleum ether/ethyl acetate=3:1) gave the title product as a colourless oil.

後処理

  1. filtrationthe precipitate was filtered off
  2. extractionThe mixture was extracted with ether
  3. washthe combined ether phases were washed with water
  4. customdried
  5. concentrationconcentrated

出典と根拠

ORDレコード
ord-92ab901a5dbc4df1b779a4bcb638b5bc
出典データセット
uspto-grants-2001_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06197729B1

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート