HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 628509Generated: October 29, 2026
Hydrochloric Acid → HCID 82112865, compound
https://huagongshe.com/reaction/628509
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-(4-Methoxy-3-methylphenyl)ethan-1-one | HCID 24806 | — |
| Catalyst | Dibenzo-18-crown-6 | HCID 26541 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 82112865 | HCID 82112865 | — |
Reaction Steps
At room temperature, to tetrahydrofuran 50 ml was added 55% sodium hydride 3.07 g and ethyl acetate 5.90 g and the resulting mixture was stirred for a half hour. Then, thereto was added 1 (4 methoxy-3-methylphenyl)-ethanone (described in Reference Preparation example 48) 5.50 g, dibenzo-18-crown-6 0.024 g and ethanol 1 ml and the resulting mixture was stirred with heating under reflux for six hours. To the reaction mixture was added water and the resulting mixture was acidified with aqueous 10% 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 1-(4-methoxy-3-methyl-phenyl)-butane-1,3-dione 6.50 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-749fad6529434d6d91c7a2230e0a1966 |
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| Source note | uspto-grants-2016_04 |
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