HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Gamma-Butyrolactone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 2,5-Dihydrofuran | HCID 15570 | — |
| Catalyst | HCID 178505374 | HCID 178505374 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | Gamma-Butyrolactone | HCID 7302 | — |
| Product | Furan | HCID 8029 | — |
| Product | 2,3-Dihydrofuran | HCID 70934 | — |
| Product | 4-Hydroxybutanal | HCID 93093 | — |
Reaction Steps
In a manner similar to that described in Example 1, 16 mL/h of 2,5-dihydrofuran and 30 mL/h of water were passed at 230° C. over 253 g of the commercially available copper chromite catalyst marketed by Suedchemie, Munich and bearing the connotation G 22 (composition according to sales brochure: 37% of Cu; 46% of Cr2O3 ; 13% of BaO; reduction in a manner similar to that described in Example 1). At a conversion of 71%, γ-butyrolactone was formed with a selectivity of 67% (2,3-dihydrofuran: 8%; furan: 3%; tetrahydrofuran: 2%; n-butanol: 1%; 4-hydroxybutyraldehyde: 0.5%; remainder: various non-analyzed low-boiling fractions).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05646307 |
| Source dataset | uspto-grants-1997_07 |
| ORD ID | ord-41eba227707c4a7fb38c30d845e22448 |
| Source note | uspto-grants-1997_07 |