HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1795753Generated: October 27, 2026
Triethylamine → 2-[(8-Difluoromethoxyquinolin-5-yl)carbonyl]-4,4,6,6-tetramethylcyclohexane-1,3,5-trione
https://huagongshe.com/reaction/1795753
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,2,4,4-Tetramethylcyclohexane-1,3,5-trione | HCID 11769166 | — |
| Reactant | 8-Difluoromethoxy-5-quinolinecarboxylic acid | HCID 22179190 | — |
| Catalyst | Trimethylsilyl cyanide | HCID 82115 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-[(8-Difluoromethoxyquinolin-5-yl)carbonyl]-4,4,6,6-tetramethylcyclohexane-1,3,5-trione | HCID 22179179 | — |
Reaction Steps
0.4 g (1.7 mmol) of 8-difluoromethoxy-5-quinolinecarboxylic acid was dissolved in 20 ml of acetonitrile, 0.4 g (1.9 mmol) of N,N-dicyclohexylcarbodiimide and 0.3 g (1.7 mmol) of 2,2,4,4-tetramethylcyclohexane-1,3,5-trione were added and the mixture was stirring at 25° C. for 20 hours. 0.4 g (4.0 mmol) of triethylamine and 2 drops of trimethylsilyl cyanide were then added, and stirring was continued at 30–35° C. for a further 3 hours. The precipitate was filtered off, and the filtrate was concentrated, 20 ml of 5% strength potassium carbonate solution were added and the mixture was washed with methyl tert-butyl ether. The aqueous phase was subsequently adjusted to pH 3 using concentrated hydrochloric acid and extracted with ethyl acetate. The solvent was removed and the residue was chromatographed over silica gel (mobile phase: methylene chloride/methanol). This gave 0.2 g of a colorless powder;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07030063B1 |
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| Source dataset | uspto-grants-2006_04 |
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| ORD ID | ord-0d8b37eaa90146c9a1e1735757c7949d |
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| Source note | uspto-grants-2006_04 |
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