Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromooctane | HCID 8140 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2,2-Diethylpropanedioate | HCID 6951563 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22468237 | HCID 22468237 | 121.7% |
Reaction Steps
To a stirring solution of diethylmalonate (16.0 g, 100 mmol) in THF (200 mL, 0.5 M) was added sodium hydride (2.4 g, 100 mmol). The solution began bubbling and an exothermic reaction occurred. The reaction eventually turned clear and then octyl bromide (17.3 mL, 100 mmol) was added. The reaction was refluxed for 20 hours and then cooled to room temperature. Another equivalent of NaH (2.4 g, 100 mmol) was added to the cloudy white mixture which was then stirred for 4 hours at room temperature. Another equivalent of octyl bromide (17.3 mL, 100 mmol) was added and the reaction was refluxed for 20 hours. The reaction was cooled to room temperature and filtered (NaBr). The mother liquor was collected and concentrated in vacuo to a yellow oil. The crude product was then distilled under vacuum (250° C.) to afford 23.4 g (64%) of pure product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06384279B1 |
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| Source dataset | uspto-grants-2002_05 |
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| ORD ID | ord-fa888faed4dc4379847898f7fa4bd333 |
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| Source note | uspto-grants-2002_05 |
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