HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalic Acid → 2-(4,6-Dimethylpyrimidin-2-yl)oxy-3,3dimethylbutyric acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalic Acid | HCID 971 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Methyl 2-(4,6-dimethylpyrimidin-2-yl)oxy3,3-dimethylbutyrate | HCID 15070275 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(4,6-Dimethylpyrimidin-2-yl)oxy-3,3dimethylbutyric acid | HCID 15070276 | 84.7% |
Reaction Steps
1.5 g of methyl 2-(4,6-dimethylpyrimidin-2-yl)oxy3,3-dimethylbutyrate was dissolved in 10 ml of methanol, and 10 ml of an aqueous solution containing 0.5 g of potassium hydroxide was added thereto. The mixture was stirred at room temperature for 12 hours and then shaked with 210 ml of toluene and 30 ml of water in a separatory funnel. The aqueous layer was acidified with an oxalic acid aqueous solution and extracted with 100 ml of ethyl ether. The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to obtain 1.2 g of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04968340 |
| Source dataset | uspto-grants-1990_11 |
| ORD ID | ord-01222139f9bc4c9bb3eb5df0f4a7f1da |
| Source note | uspto-grants-1990_11 |