Реакция #351992

ord-143e9122d6c04040b24e3efe7bb16b45

Уравнение реакции

[Na+].[Na+].[Na+].[Na+].[O-][Si]([O-])([O-])[O-]
sodium silicate
O=C([O-])[O-].[Na+].[Na+]
sodium carbonate
C1=CCOC1
2,5-dihydrofuran
[Ba]
barium
[Mg]
magnesium
[Na]
sodium
O=C([O-])[O-]
carbonate
[Mg]
magnesium
O=C1CCCO1
γ-butyrolactone
C1=COCC1
2,3-dihydrofuran
c1ccoc1
furan

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеdrying of the precipitate, extrusion to extrudates
  2. 2
    Другоеat 500° C.

Методика

In a manner similar to that described in Example 1 15 mL/h of 2,5-dihydrofuran and 32 mL/h of water were passed at 220° C. over 149 g of a catalyst containing copper and magnesium on silicon dioxide (composition: copper, calculated as Cuo: 43.0 wt %; magnesium, calculated as MgO: 18.0 wt %; silicate, calculated as SiO2 : 35.0 wt %; barium, calculated as BaO: 1 wt %; chromium, calculated as Cr2O3 : 0.6 wt %; zinc, calculated as ZnO: 0.4 wt %; sodium, calculated as Na2O: 0.2 wt %; the remainder being predominantly carbonate; all data based on the total weight of the catalyst; prepared by concurrent precipitation from a solution of the metal salts and sodium silicate (waterglass) with sodium carbonate, drying of the precipitate, extrusion to extrudates using talcum as molding auxiliary and calcination at 500° C., and reduction in a manner similar to that described in Example 1). At a conversion of 97%, γ-butyrolactone was obtained with a selectivity of 85% (2,3-dihydrofuran: 1.4%; furan: 3%; tetrahydrofuran: 9%; n-butanol: 1%; remainder: small amounts of various non-analyzed low-boiling fractions).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05646307uspto-grants-1997_07