HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 2-(Ethoxycarbonyl)-4-methylpentanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1-Ethyl 3-methyl 2-isobutylmalonate | HCID 24973459 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(Ethoxycarbonyl)-4-methylpentanoic acid | HCID 10103941 | 92.7% |
Reaction Steps
2-Isobutylmalonic acid ethyl ester methyl ester (50.0 g, 231 mmol, 1.0 eq) was dissolved into 280 ml ethanol. To this solution was added solid KOH (12.7 g, 226 mmol, 0.98 eq) and the mixture was stirred at room temperature for 16 hours. The mixture was then concentrated under reduced pressure and redissolved in 500 mL water. The solution was washed 2×250 ml diethyl ether, acidified to pH 2 with 6N HCl, and extracted with 2×250 mL diethyl ether. The organic was dried over MgSO4, and concentrated to yield intermediate (3a) (40.3 g). 1H NMR (DMSO) δ (ppm): 1.0 (dd, 6H), 1.2 (t, 1H), 1.3 (t, 3H), 1.5-1.7 (m, 1H), 1.8 (t, 2H), 3.5 (m, 2H), 4.2 (quart, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07989484B2 |
| Source dataset | uspto-grants-2011_08 |
| ORD ID | ord-3e4f1c0a64c348aaa25a42c0f3ba0213 |
| Source note | uspto-grants-2011_08 |