Cyclohexanone → HCID 178521584, Verbindung

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.

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

ORD-Eintrag

ord-b63ae0f5c959437fa391f692b89d179b

Quelldatensatz

uspto-grants-2009_09

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US07582769B2