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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 264810Generated: October 26, 2026

Sodium Carbonate → Gamma-Butyrolactone

https://huagongshe.com/reaction/264810

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2,5-DihydrofuranHCID 15570—
ReactantCarbonate IonHCID 19660—
ReactantSodium orthosilicateHCID 26051—
ReactantBariumHCID 5355457—
ReactantSodiumHCID 5360545—
ReactantMagnesiumHCID 5462224—
CatalystChromiumHCID 23976—
CatalystCopperHCID 23978—
CatalystZincHCID 23994—
SolventWaterHCID 962—
ProductGamma-ButyrolactoneHCID 7302—
ProductFuranHCID 8029—
Product2,3-DihydrofuranHCID 70934—

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05646307
Source datasetuspto-grants-1997_07
ORD IDord-143e9122d6c04040b24e3efe7bb16b45
Source noteuspto-grants-1997_07