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Hydrochloric Acid → HCID 22725156、化合物

HRID 396609
ノート
印刷プレビュー

反応式

HRID 396609 の反応式
[C:1]1([CH:7]2[CH2:12][CH2:11][N:10]([CH2:13][CH2:14][C:15]#[N:16])[CH2:9][CH2:8]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.Cl.[OH-].[Na+]>C1COCC1>[NH2:16][CH2:15][CH2:14][CH2:13][N:10]1[CH2:9][CH2:8][CH:7]([C:1]2[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=2)[CH2:12][CH2:11]1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 22725172HCID 22725172、化合物

生成物 1

HCID 22725156HCID 22725156、化合物収率 87%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

To a stirred solution of 3-(4-phenylpiperidin-1-yl)propionitrile (5.1 g, 24 mmol, 1.0 equiv) in anhydrous THF (20 mL) under argon was added a solution of BH3 in THF (1.0 M, 83 mL, 83 mmol, 3.5 equiv) at room temperature. The mixture was refluxed for 4.5 hours and then cooled to room temperature. Aqueous HCl (6 N, 130 mL) was added and stirring was continued for 2 hours at 50-70° C. The mixture was basified to pH 9 by addition of 6 N aq. NaOH and extracted with EtOAc (100 mL) and CH2Cl2 (3×100 mL). The combined organic solutions were dried over MgSO4 and concentrated. The residue was dissolved in CH2Cl2 (20 mL) and treated with HCl in ether (1.0 N, 50 mL). The solvents were removed, ether (250 mL) was added, the mixture was filtered, and the filter cake was washed with ether. Water (60 mL) was added to the resulting white solid, the pH was adjusted to 10-11 with 1 M NaOH, and the aqueous phase was extracted three times with CH2Cl2. Drying over MgSO4 followed by removal of solvents gave 4.5 g (87%) of pure product (light brown solid), which was characterized spectroscopically.

後処理

  1. temperatureThe mixture was refluxed for 4.5 hours
  2. extractionextracted with EtOAc (100 mL) and CH2Cl2 (3×100 mL)
  3. dry with materialThe combined organic solutions were dried over MgSO4
  4. concentrationconcentrated
  5. dissolutionThe residue was dissolved in CH2Cl2 (20 mL)
  6. additiontreated with HCl in ether (1.0 N, 50 mL)
  7. customThe solvents were removed
  8. additionether (250 mL) was added
  9. filtrationthe mixture was filtered
  10. washthe filter cake was washed with ether
  11. additionWater (60 mL) was added to the resulting white solid
  12. extractionthe aqueous phase was extracted three times with CH2Cl2
  13. dry with materialDrying over MgSO4
  14. customfollowed by removal of solvents

出典と根拠

ORDレコード
ord-498c47608e074215b92ca9537b839cce
出典データセット
uspto-grants-2003_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06608086B2

反応ノート

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