HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52538Generated: October 30, 2026
Toluene → 2-methyl-N-trifluoroacetyl-2-methoxycarbonyltetrahydroquinoline
https://huagongshe.com/reaction/52538
Participants
| Role | Name | HCID | Charge |
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| Reactant | Toluene | HCID 1140 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Reactant | HCID 86750626 | HCID 86750626 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-methyl-N-trifluoroacetyl-2-methoxycarbonyltetrahydroquinoline | HCID 86750627 | 98% |
Reaction Steps
To a solution of N-trifluoroacetyl-2-methoxycarbonyltetrahydroquinoline (8.7 g, 30.3 mmol)in THF (100 mL) was added slowly 0.5N potassium hexamethylsilazide in toluene (66.6 mL, 33.3 mmol) over 15 min at -78° C. The mixture was stirred for 10 min followed by addition of iodomethane (2.3 mL, 36.4 mmol) at the same temperature. The mixture was allowed to warm to room temperature, stirred 5 h, poured into water, and extracted with ethyl acetate. The extract was washed with water and brine, dried over magnesium sulfate, and concentrated to give 8.98 g of 2-methyl-N-trifluoroacetyl-2-methoxycarbonyltetrahydroquinoline (98%): 1H NMR (270 MHz, CDCl3) δ7.18 (m, 3H), 7.07 (m, 1H), 3.71 (s, 3H), 2.90 (td, 1H, J=13.9, 3.3 Hz), 2.50 (dt, 1H, J=13.9, 3.3 Hz), 2.28 (dt, 1H, J=13.9, 3.3 Hz), 1.56 (s, 3H), 1.53 (td, 1H, J=13.9, 3.3 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05616586 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-0def70cacf644c37aa161d2ee50c0060 |
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| Source note | uspto-grants-1997_04 |
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