HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1199125Generated: October 26, 2026
6-Fluoro-2,5-dimethylquinoline → 6-Fluoro-2,5-dimethyl-1,2,3,4-tetrahydroquinoline
https://huagongshe.com/reaction/1199125
Participants
| Role | Name | HCID | Charge |
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| Reactant | 6-Fluoro-2,5-dimethylquinoline | HCID 19868176 | — |
| Catalyst | Water | HCID 962 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 6-Fluoro-2,5-dimethyl-1,2,3,4-tetrahydroquinoline | HCID 13669246 | — |
Reaction Steps
7.0 kg of 2,5-dimethyl-6-fluoroquinoline, 51.5 kg of glacial acetic acid and 350 g of 50% water-wet 5% platinum on carbon catalyst were combined and hydrogenated at 50 psi for 20 hours. Gas chromatography showed residual starting material so an additional 35 g of catalyst was added and the hydrogenation was continued for an additional 2 hours. The mixture was filtered to remove the catalyst and the solvent was then evaporated. The residue was dissolved in 10 gallons of cold water, and the resulting mixture was made basic with ammonium hydroxide to pH 11 while maintaining the temperature below 30° C. The resulting mixture was extracted with 8 gallons of 1,2-dichloroethane and the extract was dried through azeotropic distillation. The dried extract was treated with magnesium sulfate and filtered, and the filtrate was concentrated in vacuo to give a dark oil, 2,5-dimethyl-6-fluoro-1,2,3,4-tetrahydroquinoline, which was used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04898945 |
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| Source dataset | uspto-grants-1990_02 |
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| ORD ID | ord-eb45be69be34467ebeee0a5717d3c717 |
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| Source note | uspto-grants-1990_02 |
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