HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 628536Generated: October 30, 2026
Hydrochloric Acid → HCID 117724717, compound
https://huagongshe.com/reaction/628536
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Carbonate | HCID 7766 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 20192689 | HCID 20192689 | — |
| Catalyst | Dibenzo-18-crown-6 | HCID 26541 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 117724717 | HCID 117724717 | 93.6% |
Reaction Steps
At room temperature, to a mixture of 1-(4-isopropoxy-3-methyl-phenyl)-ethanone (described in Reference Preparation example 93) 9.4 g and tetrahydrofuran 150 ml was added diethyl carbonate 11.6 g, 55% sodium hydride 4.5 g, dibenzo-18-crown-6 0.04 g and ethanol 3 mL, and the resulting mixture was stirred with heating under reflux for nine hours. To the reaction mixture was added water, and the resulting mixture was acidified with 10% aqueous hydrochloric acid solution and was extracted with ethyl acetate. The organic layer was washed with water and was dried over anhydrous magnesium sulfate, and was then concentrated under reduced pressure. The resulting residue was subjected to a silica gel column chromatography to give 3-(4-isopropoxy-3-methyl-phenyl)-3-oxo-propionic acid ethyl ester 12.1 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09314023B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-5b289c7a3fa4423ea2d06ee5721678f4 |
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| Source note | uspto-grants-2016_04 |
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