Tetrahydrofuran → (1R,2S,4R,5S)-Bicyclo[2.2.1]heptane-2,5-diol

Temperatur

60 °C

To (1R,2S,4R,5S)-2,5-bis(trimethoxysilyl)bicyclo[2.2.1]heptane (76.9 mmol) was added potassium hydrogen fluoride (33.0 g, 423 mmol), tetrahydrofuran (80.0 mL), methanol (80.0 mL), and urea hydrogen peroxide addition compound (65.0 g, 691 mmol, Aldrich). The resulting white slurry was stirred overnight at 60° C. After cooling to ambient temperature, MnO2 (0.56 g, 6.4 mmol) was added, and the mixture was stirred at this temperature for 4 h. The solids were removed by filtration, and the filter cake was washed with methanol. The combined filtrates were concentrated in vacuo. The residue was dissolved in water (100 mL) and extracted with a CHCl3/i-PrOH mixture (3/1, v/v, 5×100 mL). The combined organic portions were dried over MgSO4 and conc. in vacuo. After triturating the residue with CH2Cl2 and EtOAc, the white solid was collected by filtration. This material was the title compound. A second crop of desired product was obtained by flash column chromatography (0-5% MeOH in EtOAc) from the concentrated filtrate.

1. temperatureAfter cooling to ambient temperature
2. stirringthe mixture was stirred at this temperature for 4 h
3. customThe solids were removed by filtration
4. washthe filter cake was washed with methanol
5. concentrationThe combined filtrates were concentrated in vacuo
6. dissolutionThe residue was dissolved in water (100 mL)
7. extractionextracted with a CHCl3/i-PrOH mixture (3/1, v/v, 5×100 mL)
8. dry with materialThe combined organic portions were dried over MgSO4 and conc. in vacuo
9. customAfter triturating the residue with CH2Cl2 and EtOAc
10. filtrationthe white solid was collected by filtration

ORD-Eintrag

ord-760f923d5a024a4588f92c10d2224e34

Quelldatensatz

uspto-grants-2014_04

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US08686011B2