HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1417471Generated: November 4, 2026
Hydrochloric Acid → Ethyl 2-(4-oxocyclohexyl)acetate
https://huagongshe.com/reaction/1417471
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Ethyl 4-oxocyclohexylacetate ethylene acetal | HCID 67572248 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Ethyl 2-(4-oxocyclohexyl)acetate | HCID 12666966 | 96.7% |
Reaction Steps
50 ml of a 1N aqueous solution of hydrochloric acid was added to a solution of 5.0 g of ethyl 4-oxocyclohexylacetate ethylene acetal, as obtained in Example 58, in 50 ml of acetone. The reaction mixture was stirred for 10 minutes at room temperature, neutralized by the addition of a saturated aqueous solution of sodium hydrogencarbonate, and then concentrated by evaporation under reduced pressure. The resulting residue was extracted with ethyl acetate. The organic extract was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate and concentrated by evaporation under reduced pressure. The resulting residue was subjected to column chromatography using 100 g of silica gel with a 4:1 v/v mixture of hexane and ethyl acetate as the eluent, to yield 3.9 g of the title compound as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05877199 |
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| Source dataset | uspto-grants-1999_03 |
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| ORD ID | ord-f79846fd8b2a41459ed84e8bad1e9614 |
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| Source note | uspto-grants-1999_03 |
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