Reaktion #76364

ord-3c0d0e4f28e3497f83930e61cad01c92

Reaktionsgleichung

Cl
HCl
OCCCO
1,3-propanediol
CC(C)(C)[Si](C)(C)Cl
tert-butyldimethylchlorosilane
c1c[nH]cn1
imidazole
CC(C)(C)[Si](C)(C)OCCCO
product
CC(C)(C)[Si](C)(C)OCCCO
3-(tert-Butyldimethylsiloxy)-1-propanol

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Extraktionextracted with ether (3×100 mL)
  2. 2
    WaschenThe organic phases were washed with brine (100 mL)
  3. 3
    Trocknendried over anhydrous MgSO4
  4. 4
    Einengenconcentrated in vacuo
  5. 5
    SonstigeThe mixture was purified by flash chromatography

Vorschrift

A mixture of 1,3-propanediol (10 mmol), tert-butyldimethylchlorosilane (11 mmol), and imidazole (22 mmol) dissolved in 5 mL of DMF was stirred at room temperature for 16 hours. The mixture was poured into 0.1 M HCl (100 mL) and extracted with ether (3×100 mL). The organic phases were washed with brine (100 mL), dried over anhydrous MgSO4, and concentrated in vacuo. The mixture was purified by flash chromatography to give the product as a colorless oil.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06702705B1uspto-grants-2004_03