Participants
| Role | Name | HCID | Charge |
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| Reactant | Furfuryl Alcohol | HCID 7361 | — |
| Reactant | 1,4-Pentanediol carbonate | HCID 86702298 | — |
| Product | Furfuryl Alcohol | HCID 7361 | — |
| Product | HCID 86702297 | HCID 86702297 | — |
| Product | 1,4-Pentanediol carbonate | HCID 86702298 | — |
Reaction Steps
Adding 1,4-pentanediol carbonate and furfuryl alcohol in a tubular ester exchange reactor; then adding the prepared metal-rare earth oxide composite catalyst, mixing uniformly and performing an ester exchange reaction, distilling the reaction product to obtain difurfuryl carbonate, wherein the mole ratio of 1,4-pentanediol carbonate to furfuryl alcohol is 1:6, and the weight ratio of the metal-rare earth oxide composite catalyst to the total weight of 1,4-pentanediol carbonate and furfuryl alcohol is 0.5:100; the ester exchange reaction is performed at a temperature of 160° C. and under an absolute pressure of 3 MPa for 20 minutes; in the ester exchange reaction, the conversion rate of 1,4-pentanediol carbonate is 100%, and yield of difurfuryl carbonate is 92%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09045707B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-1647cb1a0f394c4199a99504f8dfb8d6 |
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| Source note | uspto-grants-2015_06 |
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