Ethylene Glycol → 2-(tert-Butyl(dimethyl)silyl)oxyethanol

Temperature

20 °C

Ethylene glycol (2.00 g) in anhydrous THF (60 ml) under nitrogen was treated portionwise with sodium hydride (60% dispersion in mineral oil, 1.29 g) and the mixture stirred at 20° C. for 45 min. Tert-butyl dimethylsilyl chloride (4.86 g) was added and the mixture stirred at 20° C. for 45 min. Phosphate buffer (60 ml, pH6.5) was added and the mixture stirred for 20 min before extracting with ether (60 ml). The organic layer was then washed with water (60 ml) and brine (60 ml), before drying over Na2SO4, filtering, and removing the solvent in vacuo. This was purified by flash chromatography on silica. Elution with 1:4 EtOAc/cyclohexane followed by solvent evaporation in vacuo gave the title compound (3.82 g). TSP+ve 194 MNH4+.

1. stirringthe mixture stirred at 20° C. for 45 min
2. stirringthe mixture stirred for 20 min
3. extractionbefore extracting with ether (60 ml)
4. washThe organic layer was then washed with water (60 ml) and brine (60 ml)
5. dry with materialbefore drying over Na2SO4
6. filtrationfiltering
7. customremoving the solvent in vacuo
8. customThis was purified by flash chromatography on silica
9. washElution with 1:4 EtOAc/cyclohexane
10. customfollowed by solvent evaporation in vacuo

ORD record

ord-97472bf81910487495da6b1ac0cb001e

Source dataset

uspto-grants-2014_04

DOI

10.6084/m9.figshare.5104873.v1

Patent number

USRE044874E1