HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569594Generated: October 27, 2026
Solketal → 4-(2,2-Dimethyl-[1,3]dioxolan-4-ylmethoxy)-3-oxo-butyric acid ethyl ester
https://huagongshe.com/reaction/569594
Participants
| Role | Name | HCID | Charge |
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| Reactant | Solketal | HCID 7528 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl 4-chloroacetoacetate | HCID 69484 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(2,2-Dimethyl-[1,3]dioxolan-4-ylmethoxy)-3-oxo-butyric acid ethyl ester | HCID 19871288 | 21.5% |
Reaction Steps
A solution of 2,2-dimethyl-4-hydroxymethyl-1,3-dioxolane (13.2 g) in tetrahydrofuran (50 ml) was added dropwise to a stirred suspension of sodium hydride (8.0 g, 60% dispersion in oil) in tetrahydrofuran (150 ml) and the mixture was then treated dropwise with a solution of ethyl 4-chloroacetoacetate (16.5 g) in tetrahydrofuran (50 ml). The mixture was stirred at room temperature overnight and evaporated. The residue was quenched with 10% aqueous acetic acid and extracted twice into dichloromethane. The combined dichloromethane extracts were washed with saturated brine, dried over MgSO4 and evaporated. The residue was purified by chromatography on SiO2 (100 g) using toluene plus 0-20% ethyl acetate as the eluant. Appropriate fractions were combined and evaporated to give the title compound (5.6 g) as an oil. This compound was used in Preparations 3 and 4 without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04732985 |
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| Source dataset | uspto-grants-1988_03 |
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| ORD ID | ord-9a6ab947ba714ae79869510e76660b63 |
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| Source note | uspto-grants-1988_03 |
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