HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488145Generated: October 28, 2026
Hydrochloric Acid → HCID 14986479, compound
https://huagongshe.com/reaction/488145
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 14986468 | HCID 14986468 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 14986479 | HCID 14986479 | 47.9% |
Reaction Steps
0.5 g of ethyl (E)-3-(4-acetoxy-3-isopropyl-5-methyl-1-naphthyl)propenoate was dissolved in 50 ml of ethanol, to which a potassium hydroxide aqueous solution (potassium hydroxide 1.6 g/water 10 ml) was added, followed by refluxing for 30 minutes. The solution was cooled to 0° C. and water was added. Dilute hydrochloric acid was added to make the aqueous phase acidic and extracted with ethyl acetate. The organic phase was washed with brine, dried with anhydrous magnesium sulfate, and concentrated in vacuo. The residue was purified by silica gel column chromatography (40% ethyl acetate/hexane) and the resultant crystals were recrystallized from a mixed solvent of isopropyl ether and ethyl acetate (1:1) and washed with isopropyl ether and hexane (3:7) to obtain 0.19 g of the titled compound as yellow needle.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05298649 |
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| Source dataset | uspto-grants-1994_03 |
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| ORD ID | ord-7a19aefef5c74ad18e8c67d5e387bc49 |
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| Source note | uspto-grants-1994_03 |
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