HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231651Generated: October 25, 2026
Ethanol → 6,8-Dichloro-3-hydroxy-2-[1,1'-biphenyl]-4-yl-4-quinolinecarboxylic acid
https://huagongshe.com/reaction/231651
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 5,7-Dichloro-1H-indole-2,3-dione | HCID 80771 | — |
| Reactant | Acetic acid 2-biphenyl-2-yl-2-oxo-ethyl ester | HCID 20034058 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6,8-Dichloro-3-hydroxy-2-[1,1'-biphenyl]-4-yl-4-quinolinecarboxylic acid | HCID 14498160 | — |
Reaction Steps
A suspension of 21 g of 5,7-dichloro-2,3-indolinedione in 120 ml of water was treated with a sufficient amount of a solution of 16.6 g 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 solid was taken up in 1500 ml of water containing 100 ml of 10N sodium hydroxide, filtered and the filtrate treated with 32 ml of concentrated hydrochloric acid and 10 ml of glacial acetic acid. The resulting solid was dissolved in 400 ml of hot cellosolve, filtered and precipitated with water, giving 18.5 g of the desired product, mp 215°-217° 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-3290670892e649a589de0ba37439b6b0 |
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| Source note | uspto-grants-1989_07 |
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