HuagongsheHuagongshe Chemistry Print Report · For research reference only
Furfural → Benzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Furfural | HCID 7362 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Diethyl Succinate | HCID 31249 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Dihydrobezofuran | HCID 5857314 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | Benzofuran | HCID 9223 | — |
Reaction Steps
As depicted in Scheme F, dihydrobenzofuran intermediate F-3 could be prepared starting from commercially available 2-furaldehyde and diethyl succinate. Treatment of 2-furaldehyde and diethyl succinate with potassium t-butoxide in refluxing t-butanol gives intermediate F-1. Treatment of F-1 with sodium acetate in refluxing acetic anhydride, followed by aqueous work-up and subsequently refluxing the residue in EtOH in the presence of K2CO3, gives benzofuran F-2. F-2 could be subjected to hydrogenation conditions to provide dihydrobenzofuran F-3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08119624B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-85cdb687fa3d4a11a8a9f11dec122a49 |
| Source note | uspto-grants-2012_02 |