Reacción #414491

ord-1fff5ed9455b47feb6e4396f27551df8

Ecuación de reacción

[Cl-].[NH4+]
ammonium chloride
B.[Na]
sodium boron hydride
C1CCOC1
tetrahydrofuran
CO
methanol
C=C1CC[C@H](CCO)[C@H]1CO
2-[(1R, 2R)-2-(hydroxymethyl)-3-methylenecyclopent-1-yl]-ethane-1-ol
Rendimiento 30.2%

Condiciones de reacción

Temperatura
80°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturathe reaction mixture was heated
  2. 2
    workup.DISTILLATIONAfter an organic solvent was once distilled off
  3. 3
    Extracciónthe aqueous layer was extracted by ethyl acetate (100 ml×3)
  4. 4
    Otrowas dried
  5. 5
    workup.ADDITIONby adding magnesium sulfate
  6. 6
    Filtraciónfiltered
  7. 7
    Concentraciónconcentrated under a reduced pressure
  8. 8
    OtroThe residual matter was purified by chromatography
  9. 9
    Otrothe solvent of the fraction obtained from ether
  10. 10
    workup.DISTILLATIONethyl acetate=3:7 eluent was distilled off
  11. 11
    OtroA colorless oily substance was thus obtained

Procedimiento

Methyl (4aS, 7aS)-1-hydroxy-7-methylene-1, 4a, 5, 6, 7a-pentahydrocyclopenta[c]pyran-4-carboxylate (2.0 g, 0.0095 mol) obtained in Example 22 wad dissolved in 40 ml of tetrahydrofuran, and after sodium boron hydride (1.8 g, 0.047 mol) was added, the reaction mixture was heated and refluxed at 80° C. 9.5 ml of methanol wad added dropwise to this solution in the course of 1 hour, and the reaction mixture was stirred further at the same temperature. 50 ml of saturated ammonium chloride solution wad added to the reaction mixture. After an organic solvent was once distilled off, the aqueous layer was extracted by ethyl acetate (100 ml×3). The organic layer was joined, and was dried by adding magnesium sulfate, filtered, and thereafter concentrated under a reduced pressure. The residual matter was purified by chromatography using silica gel, and the solvent of the fraction obtained from ether:ethyl acetate=3:7 eluent was distilled off. A colorless oily substance was thus obtained, i.e., 2-[(1R, 2R)-2-(hydroxymethyl)-3-methylenecyclopent-1-yl]-ethane-1-ol (450 mg, yield=30.2%). This 2-[(1R, 2R)-2-(hydroxymethyl)-3-methylcyclopent-1-yl]-ethane-1-ol had the following physicochemical properties:

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05272172uspto-grants-1993_12