HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49642Generated: November 1, 2026
Hydrochloric Acid → alpha-Methyl-3(2-naphthoyl)benzene Acetic Acid
https://huagongshe.com/reaction/49642
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | 7-(2-naphthoyl)-3-methyl-5,6-dihydro-2(4H)-benzofuranone | HCID 12991362 | — |
| Solvent | Water | HCID 962 | — |
| Product | alpha-Methyl-3(2-naphthoyl)benzene Acetic Acid | HCID 9901064 | — |
Reaction Steps
A mixture of 7-(2-naphthoyl)-3-methyl-5,6-dihydro-2(4H)-benzofuranone (10 g) and acetic acid potassium salt (0.3 g) was added to a reactor and stirred for 1 hr at 220° C. The reaction mixture was cooled down to room temperature. Toluene and water were added to the reaction mixture and acidified to pH 2 with 5% hydrochloric acid. Toluene layer separated was dried over anhydrous MgSO4, filtered and evaporated to give crude product. The crude product was purified by column chromatograph on silica gel by eluting with a mixture of ethylacetate and n-hexane (1:5) to give the desired product (9:42 g, 94 % .
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06706917B1 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-1f4befc33ffa492db518647e07a976d7 |
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| Source note | uspto-grants-2004_03 |
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