Reacción #1095844

ord-f6ec3c075db54f48ba5f51d59ef77176

Ecuación de reacción

CO
methanol
O=C1CCN(C(=O)OCc2ccccc2)c2ccccc21
1-benzyloxycarbonyl-2,3-dihydro-4-quinolone
[BH4-].[Na+]
sodium borohydride
C1CCOC1
tetrahydrofuran
O=C(OCc1ccccc1)N1CCC(O)c2ccccc21
1-benzyloxycarbonyl-4-hydroxy-1,2,3,4-tetrahydroquinoline
Rendimiento 95.4%

Condiciones de reacción

Temperatura
25°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrothe flask was incubated in a water bath
  2. 2
    Temperaturaout heat generation/foam formation
  3. 3
    Extracciónthe objective product was extracted
  4. 4
    LavadoFurther, the organic layer was washed with 2.5% saline
  5. 5
    workup.ADDITIONto the organic layer was added MgSO4
  6. 6
    Filtraciónthe insoluble material was filtered
  7. 7
    ConcentraciónThe filtrate was concentrated under reduced pressure

Procedimiento

To a flask were charged 25.04 g of 1-benzyloxycarbonyl-2,3-dihydro-4-quinolone, 6.72 g of sodium borohydride and 200 mL of tetrahydrofuran, and the flask was incubated in a water bath wherein the temperature was maintained constant at 25° C. To the flasks was added dropwise 50 mL of methanol over about 30 minutes with watching out heat generation/foam formation. After confirming the reaction termination by TLC, to the flask was added dropwise 400 mL of water with watching out foam formation, and to the solution was added 800 mL of ethyl acetate and the objective product was extracted. Further, the organic layer was washed with 2.5% saline, and then to the organic layer was added MgSO4, and the insoluble material was filtered. The filtrate was concentrated under reduced pressure to give 24.05 g of 1-benzyloxycarbonyl-4-hydroxy-1,2,3,4-tetrahydroquinoline as white solid (86% yield).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07972836B2uspto-grants-2011_07