HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Triphenylene-2-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Iodine | HCID 807 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Acetyltriphenylene | HCID 86641842 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | Triphenylene-2-carboxylic acid | HCID 13802081 | — |
| Product | Acetyltriphenylene | HCID 86641842 | — |
Reaction Steps
The reaction product obtained in step a) is admixed with 2.2 equivalents of I2 (based on the crude yield of acetyltriphenylene) in pyridine solvent at room temperature. Thereafter, the mixture is kept at reflux for 45 min, and then a further portion of I2 (1.0 equivalent) is added. After reflux for a further hour, NaOH, EtOH and water are added and the reaction mixture is heated to reflux for 2 h. 2-triphenylenecarboxylic acid is obtained in 76% yield (based on crude yield of acetyltriphenylene, or 74% based on triphenylene).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08455112B2 |
| Source dataset | uspto-grants-2013_06 |
| ORD ID | ord-4f10b447486b4bbc9511d7093e3fdcc6 |
| Source note | uspto-grants-2013_06 |