HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1658542Generated: October 30, 2026
Tetrahydrofuran → 5-(2-Methyl-1,3-dioxolan-2-yl)-2-pentanone
https://huagongshe.com/reaction/1658542
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Lithium | HCID 3028194 | — |
| Reactant | HCID 13551185 | HCID 13551185 | — |
| Reactant | HCID 178418348 | HCID 178418348 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 5-(2-Methyl-1,3-dioxolan-2-yl)-2-pentanone | HCID 10419628 | — |
Reaction Steps
348 Mg. of the lithium salt of the ketal acid, 4-(2-methyl-1,3-dioxolan-2-yl)butanoic acid was dissolved in 5 ml. anhydrous tetrahydrofuran. The solution was cooled to 0°C and 1.25 ml. of a 1.6 molar solution of methyllithium in diethylether was added dropwise over a period of one hour while stirring under a nitrogen atmosphere. The solution was allowed to rise approximately to 20°C and kept at this temperature over a period of 2 hours. The reaction mixture was added to crushed ice and the organic solvents were removed in vacuo. The residue was extracted with ether, the extract was washed with a saturated sodium chloride solution, dried with magnesium sulfate, filtered and evaporated in vacuo to give crude 5-(2-methyl-1,3-dioxolan-2-yl)-2-pentanone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03965117 |
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| Source dataset | uspto-grants-1976_06 |
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| ORD ID | ord-36e9656cde5240209c193557a5459675 |
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| Source note | uspto-grants-1976_06 |
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