HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1885982Generated: November 1, 2026
Hydrochloric Acid → 2-Ethoxycarbonyl-3-phenylcyclohex-5-enone
https://huagongshe.com/reaction/1885982
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl Acetoacetate | HCID 8868 | — |
| Reactant | Cinnamaldehyde | HCID 637511 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Ethoxycarbonyl-3-phenylcyclohex-5-enone | HCID 15581449 | — |
Reaction Steps
Under a nitrogen atmosphere, 0.1 gram (0.004 mole) of sodium metal was reacted in 40 mL of ethanol. The solution was stirred, and 13.0 grams (0.100 mole) of ethyl acetoacetate was added. The reaction mixture was cooled in an ice bath, and 13.2 grams (0.100 mole) of trans-cinnamaldehyde in 10 mL of ethanol was added dropwise during a 10 minute period. Upon completion of addition, the reaction mixture was allowed to warm to ambient temperature where it stirred for about 18 hours. After this time the reaction mixture was saturated with gaseous hydrochloric acid and then was allowed to stand for about 65 hours. The reaction mixture was concentrated under reduced pressure to yield 2-ethoxycarbonyl-3-phenylcyclohex-5-enone. A 100% yield (24.4 grams) of product was assumed.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05149357 |
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| Source dataset | uspto-grants-1992_09 |
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| ORD ID | ord-fa954fdf4cc1405caff67fea23cbf971 |
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| Source note | uspto-grants-1992_09 |
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