Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromopentane | HCID 7890 | — |
| Reactant | Dimethyl malonate | HCID 7943 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Sodium ethoxide | HCID 2723922 | — |
| Product | 1,3-Dimethyl 2-(1-methylbutyl)propanedioate | HCID 21678122 | — |
Reaction Steps
Sodium ethoxide was prepared from sodium metal (7.61 g) and absolute ethanol (200 ml). Dimethyl malonate (50.3 ml) was added dropwise to the ethanol containing sodium ethoxide. After heating to 80° C., 2-bromopentane (50 g) was added and the mixture was reflued for 24 h. Dimethyl (2-pentyl)malonate (62.7 g) was obtained after the usual work-up. Dimethyl (2-pentyl)malonate was added to a 50% potassium hydroxide solution and the mixture was heated for 3 h while water/ethanol being distilled off. After cooling, the solution was acidified with concentrated hydrochloric acid. Then, the solution was extracted with ethyl acetate. The extract was concentrated under reduced pressure, and the resulting product was heated to 180° C. until bubbling ceased. After distillation, colorless 3R,S-methy-caproic acid was obtained. Yield: 27.7 g (35%), b.p. 200° C./760 mmHg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05886034 |
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| Source dataset | uspto-grants-1999_03 |
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| ORD ID | ord-7cc506b55d6c463d8b7185ac902368e1 |
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| Source note | uspto-grants-1999_03 |
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