Hydrochloric Acid → HCID 70926934、化合物

HRID 576668ノート

反応式

HRID 576668 の反応式
Cl.[Br:2][C:3]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:4]=1[CH2:5][CH2:6][C@@H:7]2[OH:12].[C:13](=[O:16])([O-])O.[Na+]>C(Cl)Cl.O1C=CCCC1.O1CCOCC1>[Br:2][C:3]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:4]=1[CH2:5][CH2:6][C@@H:7]2[O:12][CH:5]1[CH2:4][CH2:3][CH2:11][CH2:13][O:16]1

参加物

7

実験手順

In methylene chloride (16.2 mL), 3,4-dihydro-2H-pyran (10.6 mL) was dissolved. To the solution, a solution of 4M hydrogen chloride in 1,4-dioxane (31.1 μL) was added and (1S)-4-bromo-2,3-dihydro-1H-inden-1-ol (10.0 g) that was commercially available or could be obtained by a known method was added. The resultant reaction mixture was stirred at room temperature for 3 hours. To the reaction mixture, a saturated aqueous sodium hydrogen carbonate solution (60 mL) was added and extracted with methylene chloride (60 mL). The organic phase was washed with brine (60 mL) and dried over anhydrous sodium sulfate. From the organic phase, the solvent was removed by evaporation under reduced pressure and the resultant residue was purified by silica gel column chromatography (eluent; n-hexane:ethyl acetate=95:5). From the eluted solution, the solvent was removed by evaporation under reduced pressure to give the title compound (15 g).

後処理

  1. customcould be obtained by a known method
  2. additionwas added
  3. customThe resultant reaction mixture
  4. extractionextracted with methylene chloride (60 mL)
  5. washThe organic phase was washed with brine (60 mL)
  6. dry with materialdried over anhydrous sodium sulfate
  7. customFrom the organic phase, the solvent was removed by evaporation under reduced pressure
  8. customthe resultant residue was purified by silica gel column chromatography (eluent; n-hexane:ethyl acetate=95:5)
  9. customFrom the eluted solution, the solvent was removed by evaporation under reduced pressure

出典と根拠

ORDレコード
ord-3cbb6ef7f0154f5b95a7384cfb1a5744
出典データセット
uspto-grants-2015_05
特許番号
US09040525B2

反応ノート

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