Réaction #44488

Équation de réaction

NH4Cl

Sodium bis(trimethylsilyl)amide

tert-butyl-chloro-dimethyl-silane

cyclooctane-1,5-diol

→

title compound

5-(tert-Butyl-dimethyl-silanyloxy)-cyclooctanol

Solvants

tetrahydrofuran

tetrahydrofuran

Conditions de réaction

Traitement

1. 1
   workup.ADDITIONAfter the addition
2. 2
   workup.STIRRINGstirred for another thirty minutes
3. 3
   TempératureThe solution was re-cooled (0° C.)
4. 4
   TempératureThe solution was then warmed to room temperature
5. 5
   workup.ADDITIONwas added
6. 6
   AutreThe mixture was partitioned with diethyl ether
7. 7
   Lavagethe organic phase was washed with brine
8. 8
   Séchagedried (MgSO4)
9. 9
   Filtrationfiltered
10. 10
    Autreevaporated
11. 11
    AutreThe residue was purified over silica gel using 2-40% ethyl acetate in hexanes

Mode opératoire

Sodium bis(trimethylsilyl)amide (76.27 mL, 1 M in tetrahydrofuran, 76.27 mmol) was added drop wise to a stirred and cooled (0° C.) solution of cyclooctane-1,5-diol (10 g, 69.34 mmol) in dry tetrahydrofuran (120 mL). After the addition, the resulting solution was warmed to room temperature and stirred for another thirty minutes. The solution was re-cooled (0° C.) and a solution of tert-butyl-chloro-dimethyl-silane (10.45 g, 69.34 mmol) in tetrahydrofuran (20 mL) was added drop wise. The solution was then warmed to room temperature and stirred overnight before an NH4Cl solution was added. The mixture was partitioned with diethyl ether, and the organic phase was washed with brine, dried (MgSO4), filtered, and evaporated. The residue was purified over silica gel using 2-40% ethyl acetate in hexanes to provide the title compound as an oil.

Source