HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → Gamma-Butyrolactone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Dimethyl maleate | HCID 5271565 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Water | HCID 962 | — |
| Product | Gamma-Butyrolactone | HCID 7302 | — |
| Product | 1,4-Butanediol | HCID 8064 | — |
Reaction Steps
The dialkyl maleate produced in the second esterification stage 13 is fed to a hydrogenation stage 17. For the hydrogenation, hydrogen 19 is also introduced into the hydrogenation stage 17. In the hydrogenation stage 17, the dimethyl maleate is reacted with the hydrogen to form tetrahydrofuran and optionally 1,4-butanediol and/or γ-butyrolactone with simultaneous formation of alkanol and water, as described, for example, in WO 88/00937, WO 91/01960, WO 03/006446 or WO 05/058855. The alkanol formed in the hydrogenation is the same alkanol as that which was introduced in the first esterification stage 9 and second esterification stage 13.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09186599B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-4bda3faa2a3f4f4fa952f63e78a6a6fc |
| Source note | uspto-grants-2015_11 |