HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Fumarate → Dimethyl Succinate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Fumarate | HCID 637568 | — |
| Reactant | Dimethyl maleate | HCID 5271565 | — |
| Reactant | HCID 22445707 | HCID 22445707 | — |
| Product | Dimethyl Succinate | HCID 7820 | — |
| Product | 4-Methylphthalic anhydride | HCID 88069 | — |
Reaction Steps
10 ml/hour of a solution of 1 mol of 5-methyl-tetrahydroisobenzofuran-1,3-dione and 2 mol of dimethyl maleate were pumped at 200° C. into the top of a trickle-phase reactor filled with 100 ml of catalyst in tablet form (5% by weight palladium-on-aluminium oxide). The conversion of the dimethyl maleate after passage through the reactor was 100%. No dimethyl fumarate could be detected in the product mixture leaving the reactor. 5-Methylisobenzofuran-1,3-dione and dimethyl succinate had been formed with selectivities of over 95% and over 97% respectively. The conversion of the dehydrogenation was 99.8%. The catalyst showed no signs of deactivation after 500 hours of operation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05672719 |
| Source dataset | uspto-grants-1997_09 |
| ORD ID | ord-381dc97d1e8449a88a854f5edccc856a |
| Source note | uspto-grants-1997_09 |