Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Ethyl formate | HCID 8025 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2,2-Dimethyloxolan-3-one | HCID 13010294 | — |
| Catalyst | Diethyl Ether | HCID 3283 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 67575852 | HCID 67575852 | 43% |
Reaction Steps
An ether solution of dihydro-2,2-dimethyl-3(2H)-furanone (4.55 g, 39.9 mmol) in 30 mL of ether was added dropwise to a suspension of sodium hydride (3.2 g of 60%, 80 mmol) in 150 mL of ether containing three drops of ethanol and 6.5 mL (80 mmol) of ethyl formate stirred at 0° C. After stirring overnight at room temperature, the reaction mixture was taken up into water, the ether layer separated, washed with additional ether, acidified with 6N HCl and with water and brine, dried over MgSO4, decolorized with charcoal, filtered and evaporated to leave 2.4 g of 4-hydroxymethylene-dihydro-2,2-dimethyl-3(2H)furanone as a colorless oil (43%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05112595 |
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| Source dataset | uspto-grants-1992_05 |
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| ORD ID | ord-dbe09df5d51249cc88c1ffbb75c6ec09 |
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| Source note | uspto-grants-1992_05 |
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