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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1645542Erstellt: 26. Oktober 2026

Dimethylformamide → 5-Benzyloxy-2,2-dimethyl-1,3-dioxane

https://huagongshe.com/reaction/1645542

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktBenzyl BromideHCID 7498—
EduktSodium hydrideHCID 24758—
Edukt2,2-Dimethyl-1,3-dioxan-5-olHCID 11029884—
KatalysatorTetrabutylammonium IodideHCID 67553—
LösungsmittelWaterHCID 962—
Produkt5-Benzyloxy-2,2-dimethyl-1,3-dioxaneHCID 2036488954,5%

Reaktionsschritte

To a N,N-dimethylformamide (200 ml) solution of the 2,2-dimethyl-1,3-dioxan-5-ol (7.1 g, 0.054 mol) obtained in the step (9a), sodium hydride, in oil (2.81 g, 0.064 mol as the content was regarded as 55%) was added at 0° C. and stirred. After benzyl bromide (12.9 ml, 0.108 mol) and tetrabutylammonium iodide (220 mg, 0.001 mol) were added at the same temperature to the mixture, the mixture was stirred at room temperature for 1.5 hours. Water was added to the reaction mixture, which was then extracted with ethyl acetate three times. Organic layers were combined, washed five times with water and once with a saturated saline solution, dried over anhydrous sodium sulfate, and filtered. After NH silica gel was added, the resultant mixture was concentrated and purified by silica gel column chromatography (elution solvent: heptane, heptane/ethyl acetate=9/1, 4/1, ethyl acetate) to obtain the title compound (6.5 g, 54.5%) as a colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08124780B2
Quelldatensatzuspto-grants-2012_02
ORD IDord-3ed6ca2a0d234cbb978cc9a7de249aba
Quellennotizuspto-grants-2012_02