HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231652Generated: October 25, 2026
Ethanol → 3-Hydroxy-8-methyl-2-[1,1'-biphenyl]-4-yl-4-quinolinecarboxylic acid
https://huagongshe.com/reaction/231652
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 7-Methylisatin | HCID 14313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Acetic acid 2-biphenyl-2-yl-2-oxo-ethyl ester | HCID 20034058 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Hydroxy-8-methyl-2-[1,1'-biphenyl]-4-yl-4-quinolinecarboxylic acid | HCID 14498161 | — |
Reaction Steps
A suspension of 16.1 g of 7-methyl-2,3-indolinedione in 120 ml of water was treated with a sufficient amount of a solution of 16.6 of sodium hydroxide in 55 ml of water to provide solution. A warm solution of 25.4 g of acetoxyacetylbiphenyl in 350 ml of ethanol was added, followed by the balance of the alkali solution. The mixture was refluxed for 2.5 hours. During the last 1/2 hour 50 ml of ethanol was distilled off. A 300 ml portion of water was added, the mixture was stirred, cooled and filtered through diatomaceous earth. The filtrate was treated with 34 ml of concentrated hydrochloric acid and 12 ml of glacial acetic acid. The resulting solid was collected and recrystallized from ethanol/water, giving 13.6 g of the desired product, mp 178°-180° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04847381 |
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| Source dataset | uspto-grants-1989_07 |
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| ORD ID | ord-f5040293352c4e43911d9656c29a5a6a |
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| Source note | uspto-grants-1989_07 |
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