HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339164Generated: October 29, 2026
Ethyl 2-methylacetoacetate → HCID 57614922, compound
https://huagongshe.com/reaction/339164
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 2-methylacetoacetate | HCID 701 | — |
| Reactant | Propane sultone | HCID 14264 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57614922 | HCID 57614922 | — |
Reaction Steps
Sodium hydride (2.1 g, 80 wt %=69 mmol) was slurried in 10 ml dry THF. The suspension was cooled to 0° C. and a solution of ethyl-2-methylacetoacetate (10 g, 69 mmol) in 10 ml dry THF was added dropwise. The solution was stirred at room temperature for one h. A solution of 1,3-propanesultone (8.42 g, 69 mmol) in 10 ml dry THF was added dropwise. Once the addition was complete, the solution was stirred for two h at 40° C. The solution was evaporated to dryness. The residue was dissolved in 100 ml water. The aqueous solution was extracted twice with ethylacetate, then 100 ml concentrated HCl was added and the solution was refluxed for two hours. The solvent was evaporated in vacuum. The residue was purified by column chromatography (silica, methanol/dichloromethane) to give 4-methyl-5-oxohexane sulfonic acid. Yield 10 g; MS (ESI−): 193.2 [M]−
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08889884B1 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-9fc0663ecad5424b98bc57056aea8a28 |
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| Source note | uspto-grants-2014_11 |
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