HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2381294Generated: November 4, 2026
Potassium Hydroxide → 2-(2-Ethylbutyl)malonic acid
https://huagongshe.com/reaction/2381294
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 5049261 | HCID 5049261 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(2-Ethylbutyl)malonic acid | HCID 22059000 | 96.7% |
Reaction Steps
A solution of 2-(2-ethyl-butyl)-malonic acid diethyl ester (4.78 g, 19.5 mmol) in ethanol (43.5 mL) was treated with a solution of potassium hydroxide (3.3 g, 58.7 mmol) in water (10.9 mL). The reaction was then heated to 105° C. for 6 h. After this time, the reaction was concentrated in vacuo. The residue was diluted with water (50 mL) which was then acidified with a 2N aqueous hydrochloric acid solution and then extracted with a 90/10 methylene chloride/methanol solution (3×50 mL). The combined organics were dried over sodium sulfate, filtered and concentrated in vacuo to afford 2-(2-ethyl-butyl)-malonic acid (3.55 g, 96%) as an off-white solid, which was used without further purification; EI+-HRMS m/e calcd for C9H16O4 [M+Na]+ 211.0941, found 211.0941. 1H NMR (300 MHz, DMSO-d6) δ ppm 0.79 (t, J=7.4 Hz, 6H) 1.09-1.39 (m, 5H) 1.65 (t, J=7.1 Hz, 2H) 3.22 (t, J=7.5 Hz, 1H) 12.65 (br. s., 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08258134B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-7d35d789dd31491e811122f3a699b621 |
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| Source note | uspto-grants-2012_09 |
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