Potassium Carbonate → HCID 20429506、化合物

HRID 354690

反応式

HRID 354690 の反応式
[Cl:1][C:2]1[CH:15]=[CH:14][C:5]2[C:6]3[CH:12]=[CH:11][C:10]([OH:13])=[CH:9][C:7]=3[O:8][C:4]=2[CH:3]=1.[C:16](=O)([O-])[O-].[K+].[K+].Br[C:23]([Br:26])([CH3:25])C>C(C(C)=O)C>[Br:26][CH2:23][CH2:25][CH2:16][O:13][C:10]1[CH:11]=[CH:12][C:6]2[C:5]3[CH:14]=[CH:15][C:2]([Cl:1])=[CH:3][C:4]=3[O:8][C:7]=2[CH:9]=1

参加物

5

実験手順

A mixture of 98.4 g (0.45 mole) of 7-chlorodibenzofuran-3-ol, 200 ml of methyl ethyl ketone, 93 g (0.67 mole) of potassium carbonate and 283 g (1.4 moles) of dibromopropane was refluxed for 24 hours. The inorganic precipitate was filtered off with suction and the filtrate was concentrated under reduced pressure. The residue was dissolved in 500 ml of methylene chloride and the solution was washed with 100 ml of water, 100 ml of 2 N sodium hydroxide solution and 100 ml of water in succession, dried over sodium sulfate and concentrated under reduced pressure. The solid residue was left to stand with 30 ml of pentane at 0° C. for 30 minutes, filtered off with suction and washed with 30 ml of cold n-pentane. 77 g of pure 1-bromo-3-(7-chlorodibenzofuran-3-oxy)-propane of melting point 83°-85° C. were obtained; yield: 50% of theory.

後処理

  1. temperaturewas refluxed for 24 hours
  2. filtrationThe inorganic precipitate was filtered off with suction
  3. concentrationthe filtrate was concentrated under reduced pressure
  4. dissolutionThe residue was dissolved in 500 ml of methylene chloride
  5. washthe solution was washed with 100 ml of water, 100 ml of 2 N sodium hydroxide solution and 100 ml of water in succession
  6. dry with materialdried over sodium sulfate
  7. concentrationconcentrated under reduced pressure
  8. waitThe solid residue was left
  9. filtrationfiltered off with suction
  10. washwashed with 30 ml of cold n-pentane

出典と根拠

ORDレコード
ord-53aae8a75c18456fa8b709f87e828e9f
出典データセット
uspto-grants-1983_03
特許番号
US04376776

関連ノート

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