Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 20081053 | HCID 20081053 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 20081056 | HCID 20081056 | 58.4% |
Reaction Steps
A solution of 4,5-diethoxycarbonyl-2-ethyl-2-methyl-1,3-dioxolane (13.68 g, 52.6 mmol) in dry ether (80 ml) was added dropwise over 30 min to a suspension of lithiumaluminiumhydride (2.4 g, 63.2 mmol) in dry ether (100 ml) and the mixture was refluxed under nitrogen for 2 h then stirred at room temperature overnight then refluxed for 2 further hours. On cooling, water (2.5 ml), sodium hydroxide (4N, 2.5 ml) and water (25 ml) were sequentially added cautiously down the condenser. The supernatant was decanted off and the residue was triturated with ether (2×100 ml). The combined ether layers were dried over sodium sulfate, filtered and evaporated to dryness. The residue was distilled under high vacuum (approx. 2 mm, 160 deg.) to give the title compound as a clear oil (5.41 g, 58%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05401378 |
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| Source dataset | uspto-grants-1995_03 |
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| ORD ID | ord-ea747adc0db74ceb99a5e06222ffa803 |
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| Source note | uspto-grants-1995_03 |
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