Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 19105292 | HCID 19105292 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 19105284 | HCID 19105284 | 69.3% |
Reaction Steps
A mixture of ethyl 6-chloro-4-(3,5-di-tert-butyl-4-hydroxyphenyl)-2-oxo-2H-1-benzopyran-3-carboxylate (2.0 g), 2N NaOH (11 ml) and ethanol (20 ml) was heated at 70° C. for 10 minutes. Then, the mixture was made acid with 2N HCl and extracted with ethyl acetate. The extract was washed with water and dried (MgSO4), and then, the solvent was removed to obtain 6-chloro-4-(3,5-di-tert-butyl-4-hydroxyphenyl)-2-oxo-2H-1-benzopyran-3-carboxylic acid as powders (1.3 g, 69.1%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05278186 |
|---|
| Source dataset | uspto-grants-1994_01 |
|---|
| ORD ID | ord-356ec795a30442c1aca5cc077fef45f3 |
|---|
| Source note | uspto-grants-1994_01 |
|---|