HuagongsheHuagongshe Chemistry Print Report · For research reference only
P-Xylene → HCID 10915107, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | P-Xylene | HCID 7809 | — |
| Reactant | 5,7-Di-tert-butyl-3-hydroxy-2-benzofuranone | HCID 6850821 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 10915107 | HCID 10915107 | 80.1% |
Reaction Steps
To a solution of 262.3 g (1.00 mol) of 5,7-di-tert-butyl-3-hydroxy-3H-benzofuran-2-one (compound (201), Table 2, Example 1a) in 500 ml (4.05 mol) of p-xylene are added 40 g of Fulcat 22B and the mixture is refluxed for 1.5 hours on a water separator. The Fulcat 22B catalyst is then removed by filtration and excess p-xylene is removed by distillation on a vacuum rotaray evaporator. Crystallization of the residue from 400 ml of methanol yields 280.6 g (80%) of 5,7-di-tert-butyl-3-(2,5-dimethylphenyl)-3H-benzofuran-2-one, m.p. 93°-97° C. (compound (101), Table 1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05516920 |
| Source dataset | uspto-grants-1996_05 |
| ORD ID | ord-a295a0bb80fd4250943842f2c91a8633 |
| Source note | uspto-grants-1996_05 |