Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507991Generated: October 25, 2026

Dimethylformamide → methyl 4-[(2-methyl-3,4-dihydroquinolin-1(2H)-yl)methyl]-3-[(methylsulfonyl)oxy]benzoate

https://huagongshe.com/reaction/507991

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Methyl-1,2,3,4-tetrahydroquinolineHCID 96289—
ReactantMethyl 4-(bromomethyl)-3-[(methylsulfonyl)oxy]benzoateHCID 23157330—
SolventEthyl AcetateHCID 8857—
Productmethyl 4-[(2-methyl-3,4-dihydroquinolin-1(2H)-yl)methyl]-3-[(methylsulfonyl)oxy]benzoateHCID 2315748875%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of methyl 4-(bromomethyl)-3-[(methylsulfonyl)oxy]benzoate (0.70 g, 2.2 mmol), 2-methyl-1,2,3,4-tetrahydroquinoline (0.39 g, 2.6 mmol), potassium carbonate (0.60 g, 4.3 mmol) and N,N-dimethylformamide (14 mL) was stirred at 70° C. for 23 hr. The reaction mixture was diluted with ethyl acetate, washed with water and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=10/1-2/1) to give the title compound (0.63 g, yield 75%) as a pale-yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786165B2
Source datasetuspto-grants-2010_08
ORD IDord-6312856ef23848778fe07efbc22e69ae
Source noteuspto-grants-2010_08