HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 973343Generated: October 29, 2026
Potassium Iodide → Diethyl 2-(5-acetoxypentyl)-2-methylmalonate
https://huagongshe.com/reaction/973343
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Diethyl methylmalonate | HCID 11857 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-CHLOROPHENYL ACETATE | HCID 83061 | — |
| Product | Diethyl 2-(5-acetoxypentyl)-2-methylmalonate | HCID 54079282 | — |
Reaction Steps
Sodium hydride (4.8 g., 0.2 mole) as a 50% suspension in mineral oil is washed with petroleum ether under nitrogen to remove the mineral oil, suspended in dry benzene (150 ml.), and the suspension cooled in an ice bath. Diethyl methylmalonate (34.8 g., 0.2 mole) dissolved in sieve dried DMF (150 ml.) is added to the suspension of sodium hydride dropwise. The mixture is allowed to stand overnight at room temperature. Potassium iodide (0.4 g.) and 5-acetoxyphenyl chloride (32.9 g., 0.2 mole) are then added, and the mixture is heated for 24 hours at 125° in an oil bath. The reaction mixture is concentrated in vacuo, diluted with ether (200 ml.), and filtered to remove sodium chloride. The filtrate is washed with brine, dried over anhydrous magnesium sulfate and concentrated to yield 39.6 g. (66%) of oily product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04055597 |
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| Source dataset | uspto-grants-1977_10 |
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| ORD ID | ord-9a80df9c3e55467d8d15e0734c6ecf9a |
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| Source note | uspto-grants-1977_10 |
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