HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → HCID 22507796, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 5,7-Di-tert-butyl-3-hydroxy-2-benzofuranone | HCID 6850821 | — |
| Reactant | HCID 18620266 | HCID 18620266 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22507796 | HCID 22507796 | 26.3% |
Reaction Steps
3.8 g (0.0146 mol) of 5,7-di-tert-butyl-3-hydroxy-benzofuranone, 6.1 g (0.032 mol) of p-toluenesulfonic acid and 6.9 g (0.032 mol) of 4-acetamino-tetramethylpiperidine (TEMPO) are stirred in 100 ml of dichloromethane at room temperature for 24 hours. The yellow solution is then washed three times with 200 ml of 5% hydrochloric acid each time, dried over magnesium sulfate and concentrated to dryness by evaporation. Crystallisation of the residue from hexane yields 1 g of the above-mentioned compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06533825B2 |
| Source dataset | uspto-grants-2003_03 |
| ORD ID | ord-2a4801e29a714bc4a8dd603acbd41104 |
| Source note | uspto-grants-2003_03 |