HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → 2,5-Dimethyl-3-furancarboxanilide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Acetoacetanilide | HCID 7592 | — |
| Reactant | 2-(Acetyloxy)propanal | HCID 90728 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2,5-Dimethyl-3-furancarboxanilide | HCID 34281 | — |
Reaction Steps
A solution of 24 parts of α-acetoxypropionaldehyde, 35.4 parts of acetoacetanilide and 2 parts of p-toluenesulfonic acid in 100 parts of benzene is kept for 3 hours at 40° C and then boiled under reflux for 1 hour. Adopting the isolation procedure described in Example 1 there is obtained 41.8 parts of 2,5-dimethylfuran-3-carboxanilide having a melting point of 92° to 93° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04013684 |
| Source dataset | uspto-grants-1977_03 |
| ORD ID | ord-5f59a1c4dbd54bfb931d73bada34606e |
| Source note | uspto-grants-1977_03 |