Cyclohexanone → HCID 178521584、化合物

HRID 731487

反応式

HRID 731487 の反応式
Cl.[NH2:2][C@@H:3]1[CH2:8][CH2:7][C@H:6]([OH:9])[CH2:5][CH2:4]1.[C:10]1(=O)[CH2:15][CH2:14][CH2:13][CH2:12][CH2:11]1.[BH3-]C#N.[Na+].[BH4-].[Na+]>CO.CC(O)=O>[CH:10]1([NH:2][C@H:3]2[CH2:8][CH2:7][C@@H:6]([OH:9])[CH2:5][CH2:4]2)[CH2:15][CH2:14][CH2:13][CH2:12][CH2:11]1

参加物

7

実験手順

A mixture of cis-4-aminocyclohexanol hydrochloride (4 mmol) and cyclohexanone (8 mmol) and molecular sieves (3 Å, 1 g) in anhydrous MeOH (10 mL) was stirred under N2 at room temperature for 10 min. The mixture was added NaBH3CN (8 mmol) and glacial AcOH (0.1 mL) and stirred for further 24 h. Addition of NaBH4 (1.3 mmol) followed by stirring for another 10 min. The mixture was filtered and the residue was extracted with MeOH (10 mL) and the combined filtrates were evaporated to dryness. The residue was dissolved in 1 M aqueous HCl (15 mL) and washed with TBME (15 mL). The aqueous phase was added 10% aqueous NaOH until pH 14 and extracted with TBME (15 mL). The organic phase was washed with H2O (10 ml), dried (Na2SO4), and evaporated to dryness under reduced pressure affording crude cyclohexyl-cis-(4-hydroxycyclohexyl)amine which was used in the next step without further purification.

後処理

  1. stirringstirred for further 24 h
  2. stirringby stirring for another 10 min
  3. filtrationThe mixture was filtered
  4. extractionthe residue was extracted with MeOH (10 mL)
  5. customthe combined filtrates were evaporated to dryness
  6. dissolutionThe residue was dissolved in 1 M aqueous HCl (15 mL)
  7. washwashed with TBME (15 mL)
  8. additionThe aqueous phase was added 10% aqueous NaOH until pH 14
  9. extractionextracted with TBME (15 mL)
  10. washThe organic phase was washed with H2O (10 ml)
  11. dry with materialdried (Na2SO4)
  12. customevaporated to dryness under reduced pressure

出典と根拠

ORDレコード
ord-b63ae0f5c959437fa391f692b89d179b
出典データセット
uspto-grants-2009_09
特許番号
US07582769B2

関連ノート

読み込み中…