HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,4-Di-tert-butylphenol → 5,7-Di-tert-butyl-3-(4-hydroxyphenyl)benzofuran-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,4-Di-tert-butylphenol | HCID 7311 | — |
| Reactant | 2-Hydroxy-2-(4-hydroxyphenyl)acetic acid hydrate | HCID 12677290 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 5,7-Di-tert-butyl-3-(4-hydroxyphenyl)benzofuran-2-one | HCID 18991413 | 57% |
Reaction Steps
A mixture of 103.2 g (0.50 mol) of 2,4-di-tert-butylphenol and 102.4 g (0.55 mol) of 4-hydroxymandelic acid monohydrate in 100 ml of acetic acid is refluxed under a nitrogen atmosphere for 24 hours. The reaction mixture is then diluted with 140 ml of 50% aqueous acetic acid, cooled, and the precipitate formed is filtered off. The residue is washed with a further 200 ml of 50% aqueous acetic acid and then dried to give 95.9 g (57%) of 5,7-di-tert-butyl-3-(4-hydroxyphenyl)benzofuran-2-one, m.p. 187°-190° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05428162 |
| Source dataset | uspto-grants-1995_06 |
| ORD ID | ord-f35201ee5fb44d3c832433c8e0210412 |
| Source note | uspto-grants-1995_06 |