Réaction #215692

ord-84479a15490745829d5c3b760057b4ea

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autreare placed together at 0° C
  2. 2
    AutreThe suspension obtained
  3. 3
    Filtrationfiltered
  4. 4
    LavageThe crystals were rinsed thoroughly with ether/n-hexane 1:1 (200 ml)
  5. 5
    LavageThe filtrate was washed in succession with water (2×700 ml) and saturated aqueous sodium chloride solution (500 ml)
  6. 6
    Séchagedried over magnesium sulphate
  7. 7
    Concentrationconcentrated
  8. 8
    AutreThe oil obtained
  9. 9
    workup.DISTILLATIONwas distilled over a Vigreux column (7.5 cm)

Mode opératoire

n-Butyl glycolate (231 g; 1.75 mol) and imidazole (345.1 g; 5.07 mol) are placed together at 0° C. The suspension obtained was treated portionwise with t-butyldimethylchlorosilane (303 g; 2.01 mol) during 1.5 hours. After 20 hours at room temperature the reaction mixture was diluted with ether/n-hexane 1:1 (1 l) and suction filtered. The crystals were rinsed thoroughly with ether/n-hexane 1:1 (200 ml). The filtrate was washed in succession with water (2×700 ml) and saturated aqueous sodium chloride solution (500 ml), dried over magnesium sulphate and concentrated. The oil obtained was distilled over a Vigreux column (7.5 cm). Yield: 405 g (94%) as a colourless oil (b.p. 78° C./0.98 mmHg).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05464617uspto-grants-1995_11