HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 2-(2,5-Dimethylphenyl)-2-hydroxyacetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Diethyl 2-(2,5-dimethylphenyl)-2-hydroxymalonate | HCID 12836549 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(2,5-Dimethylphenyl)-2-hydroxyacetic acid | HCID 277662 | — |
Reaction Steps
A sample of the diethyl (2,5-dimethylphenyl)-hydroxymalonate (21 parts) was reacted with a solution of potassium hydroxide (21 parts) in water (84 parts) at 98° C. for 5 hours. After cooling to ambient temperature, the reaction was washed with diethyl ether and acidified with 10M hydrochloric acid. After heating to 98° C. for a further 2 hours, the cooled materials was extracted into diethyl ether. The separated organic phase was dried over magnesium sulfate, filtered and the solvent was evaporated under reduced pressure. The crude amber coloured oil (15 parts) solidified on standing. Recrystallisation from toluene gave 2,5-dimethylmandelic acid (7 parts). The 1Hnmr, 13Cnmr and mass spectra were all consistent with the structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05717112 |
| Source dataset | uspto-grants-1998_02 |
| ORD ID | ord-99c38457053b4093846e6cd5f156bc32 |
| Source note | uspto-grants-1998_02 |