HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1678913Generated: October 29, 2026
Tetrahydrofuran → 5-(2-Methyl-1,3-dioxolan-2-yl)-2-pentanone
https://huagongshe.com/reaction/1678913
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 two 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 | US04077983 |
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| Source dataset | uspto-grants-1978_03 |
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| ORD ID | ord-32b8d853b1d34b06ac07b38924db228c |
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| Source note | uspto-grants-1978_03 |
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