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Water → HCID 21990154、化合物

HRID 7460
ノート
印刷プレビュー

反応式

HRID 7460 の反応式
Br[CH2:2][C:3]([C:5]1[CH:10]=[C:9]([CH2:11][CH2:12][OH:13])[C:8]([O:14][CH3:15])=[CH:7][C:6]=1[OH:16])=O.C([O-])(=O)C.[Na+].O.C(OCC)(=O)C>CO>[CH3:15][O:14][C:8]1[C:9]([CH2:11][CH2:12][OH:13])=[CH:10][C:5]2[CH:3]=[CH:2][O:16][C:6]=2[CH:7]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 962WaterHCID 8857Ethyl AcetateHCID 517045Sodium AcetateHCID 21990092HCID 21990092、化合物

生成物 1

HCID 21990154HCID 21990154、化合物収率 13.6%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

In 70 mL of methanol was dissolved 16.4 g of the aforesaid 2-bromo-1-[2-hydroxy-5-(2-hydroxyethyl)-4-methoxyphenyl]-1-ethanone, and 17.3 g of sodium acetate was added to the solution, after which the resulting mixture was heated under reflux for 5 minutes. After the reaction mixture was cooled, water and ethyl acetate were added thereto and the organic layer was separated. The organic layer was washed with water and then a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and then distilled under reduced pressure to remove the solvent. The residue was dissolved in 150 mL of methanol and to the resulting solution was added 6.30 g of sodium borohydride in small portions, after which the resulting mixture was stirred at room temperature for 1 hour. Then, the resulting solution was adjusted to pH 1 with 6 mol/L hydrochloric acid and stirred at room temperature for another 1 hour. The reaction mixture was concentrated under reduced pressure and water and ethyl acetate were added thereto, after which the organic layer was separated. The organic layer was washed with water and then a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and then distilled under reduced pressure to remove the solvent. The residue was purified by a column chromatography (eluent; hexane:ethyl acetate=4:1) to obtain 1.48 g of 2-(6-methoxy-1-benzofuran-5-yl)-1-ethanol as light-yellow crystals.

後処理

  1. additionwas added to the solution
  2. temperatureafter which the resulting mixture was heated
  3. temperatureunder reflux for 5 minutes
  4. temperatureAfter the reaction mixture was cooled
  5. customthe organic layer was separated
  6. washThe organic layer was washed with water
  7. dry with materiala saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate
  8. distillationdistilled under reduced pressure
  9. customto remove the solvent
  10. dissolutionThe residue was dissolved in 150 mL of methanol and to the resulting solution
  11. additionwas added 6.30 g of sodium borohydride in small portions
  12. stirringstirred at room temperature for another 1 hour
  13. concentrationThe reaction mixture was concentrated under reduced pressure and water and ethyl acetate
  14. additionwere added
  15. customafter which the organic layer was separated
  16. washThe organic layer was washed with water
  17. dry with materiala saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate
  18. distillationdistilled under reduced pressure
  19. customto remove the solvent
  20. customThe residue was purified by a column chromatography (eluent; hexane:ethyl acetate=4:1)

出典と根拠

ORDレコード
ord-8991ecdc659942da8003d54feb40c8a9
出典データセット
uspto-grants-2006_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07087594B2

反応ノート

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