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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantMethyl iodideHCID 6328—
ReactantPotassiumHCID 5462222—
ReactantHCID 86750626HCID 86750626—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-methyl-N-trifluoroacetyl-2-methoxycarbonyltetrahydroquinolineHCID 8675062798%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05616586
Source datasetuspto-grants-1997_04
ORD IDord-0def70cacf644c37aa161d2ee50c0060
Source noteuspto-grants-1997_04