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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1679032Erstellt: 26. Oktober 2026

Diethyl Ether → 2-Methyl-1,3-bis(2-tetrahydropyranyloxy)-2-propanol

https://huagongshe.com/reaction/1679032

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl EtherHCID 3283—
Edukt2-Propanone, 1,3-bis[(tetrahydro-2H-pyran-2-yl)oxy]-HCID 11010660—
EduktHCID 178418573HCID 178418573—
Produkt2-Methyl-1,3-bis(2-tetrahydropyranyloxy)-2-propanolHCID 20364956—
ProduktHCID 178418573HCID 178418573—

Reaktionsschritte

A solution of 0.14 moles of methylmagnesium bromide in diethyl ether was prepared by dissolving 15.5 g of 3M methylmagnesium bromide solution (in diethyl ether) in 100 ml of specially dried diethyl ether. While stirring at 25°-30° , a solution of 25.8 g of 1,3-bis(2-tetrahydropyranyloxy)-2-propanone, prepared as above, in 100 ml of diethyl ether was added dropwise. A white solid separated and refluxing occurred. The mixture was warmed to maintain reflux for 1 hour, then allowed to stand for 16 hours. Saturated ammonium chloride solution (100 ml) was added very slowly and when addition was completed, the layers were separated. The aqueous layer was extracted (2 × 100 ml) with diethyl ether. The ether solutions were combined, washed (2 × 100 ml) with water and dried over magnesium sulfate. The dried solution was concentrated and distilled to give 16.2 g of 2-methyl-1,3-bis(2-tetrahydropyranyloxy)-2-propanol, b.p. 121°-136°/2--3 × 10- 4 mm.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04077982
Quelldatensatzuspto-grants-1978_03
ORD IDord-6917cffd08e9425a8a3b00957876d8da
Quellennotizuspto-grants-1978_03