HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1598646Generated: October 26, 2026
Hydrochloric Acid → 4,5,8-Trimethyl-6-nitroquinoline
https://huagongshe.com/reaction/1598646
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Nitro-2,5-xylidine | HCID 18963 | — |
| Reactant | 4-Methoxybutan-2-one-dimethylacetal | HCID 81084 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4,5,8-Trimethyl-6-nitroquinoline | HCID 10560662 | — |
Reaction Steps
A mixture of 2,5-dimethyl-4-nitroaniline (0.96 g), ferric chloride hexahydrate (2.50 g), zinc chloride (0.094 g), concentrated hydrochloric acid (0.481 mL), and ethanol (8 mL) is heated to 60° C. 1,3,3-trimethoxybutane (0.73 mL) is added dropwise while the reaction mixture is kept at 60° C. The reaction mixture is heated at reflux overnight and cooled to room temperature. A solution of 10% aqueous sodium hydroxide is added, and the mixture is extracted three times with methylene chloride. The combined organic layers are dried over sodium sulfate, filtered and evaporated to afford a crude product. The crude product is purified by flash chromatography using 25% ethyl acetate in hexane as eluent, providing 6-nitro-4,5,8-trimethylquinoline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05739148 |
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| Source dataset | uspto-grants-1998_04 |
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| ORD ID | ord-5232e5899cfb43e38c3858ee8996cd17 |
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| Source note | uspto-grants-1998_04 |
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