HuagongsheHuagongshe Chemistry Print Report · For research reference only
Glyoxylic Acid → 7-tert-butyl-3-hydroxy-5-methyl-3H-benzofuran-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Glyoxylic Acid | HCID 760 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 2-tert-Butyl-4-methylphenol | HCID 17004 | — |
| Catalyst | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 7-tert-butyl-3-hydroxy-5-methyl-3H-benzofuran-2-one | HCID 18620268 | 82% |
Reaction Steps
A mixture of 49.8 g (0.30 mol) of 2-tert-butyl-4-methylphenol, 48.9 g (0.33 mol) of 50% aqueous glyoxylic acid and 0.15 g (0.79 mmol) of p-toluenesulfonic acid monohydrate in 90 ml of 1,2-dichloroethane is refluxed under nitrogen for 3.5 hours on a water separator. The reaction mixture is afterwards cooled to +5° C. and the precipitate is isolated by filtration and washed with cold 1,2-dichloroethane. The filter residue is dried under a high vacuum at room temperature, affording 54.0 g (82%) of 7-tert-butyl-3-hydroxy-5-methyl-3H-benzofuran-2-one, m.p. 152°-160° C. (compound (102), Table 1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05614572 |
| Source dataset | uspto-grants-1997_03 |
| ORD ID | ord-4569e822bdc645b8ae1d2914c1a38408 |
| Source note | uspto-grants-1997_03 |