HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Hydroxy[bis(4-methylphenyl)]acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Di-p-tolylhydroxyacetic acid methyl ester | HCID 22574226 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Hydroxy[bis(4-methylphenyl)]acetic acid | HCID 229097 | — |
Reaction Steps
A solution of 22 (613 mg, 2.26 mmol) in methanol (75 mL) was treated with 1 N NaOH (10 mL) at room temperature. The mixture was stirred at room temperature overnight. The mixture was neutralized with 1 N HCl and the solvent was removed in vacuo. The residue was dissolved in dichloromethane and 1 N HCl solution. The aqueous layer was extracted with two additional portions of dichloromethane and the combined organic extracts were washed with brine, dried over Na2SO4, and concentrated under reduced pressure to afford the title compound (23). The crude product was used directly.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06274583B1 |
| Source dataset | uspto-grants-2001_08 |
| ORD ID | ord-c9934354e9db41dabc53da71157381a1 |
| Source note | uspto-grants-2001_08 |