HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → (2R)-2-hydroxy-2-(2-methoxyphenyl)acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 167820-07-7 | HCID 45114263 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (2R)-2-hydroxy-2-(2-methoxyphenyl)acetic acid | HCID 53887132 | 62.4% |
Reaction Steps
To a solution of 19 g of methyl (2R)-2-(methoxyphenyl)-2-hydroxyethanoate (cf. Journal of Chemical Society, Parkintrans 1, 2253–2255 (1992)) in 50 ml of methanol, 50 ml of 3N aqueous sodium hydroxide solution was added, followed by 12 hours' stirring at room temperature. Distilling the methanol off under reduced pressure, the reaction liquid was acidified with 1N hydrochloric acid and extracted with chloroform. The organic layer was dried over anhydrous sodium sulfate and the solvent was distilled off under reduced pressure, to provide 11 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07192969B2 |
| Source dataset | uspto-grants-2007_03 |
| ORD ID | ord-a5ffd641a7f64176b44e30e1a178e266 |
| Source note | uspto-grants-2007_03 |