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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604011Generated: October 25, 2026

Ethyl Acetate → 2-(Cyclopropylmethyl-propyl-amino)-5-trifluoromethyl-benzaldehyde

https://huagongshe.com/reaction/604011

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
ReactantCyclopropanemethanamine, N-propyl-HCID 117787—
Reactant2-Fluoro-5-(trifluoromethyl)benzaldehydeHCID 2734904—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product2-(Cyclopropylmethyl-propyl-amino)-5-trifluoromethyl-benzaldehydeHCID 8662676988.1%

Reaction Conditions

Temperature120 °C

Reaction Steps

2-Fluoro-5-trifluoromethyl-benzaldehyde (1.3 g) and cyclopropylmethyl-propyl-amine (1.15 g) are dissolved in toluene (13 ml), and thereto is added potassium carbonate (2.81 g) and the mixture is stirred at 120° C. overnight. The reaction solution is cooled to room temperature, and thereto are added ethyl acetate and water, and the mixture is separated, and the organic layer is washed with a saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. The resulting residue is purified by silica gel column chromatography (hexane:ethyl acetate=1:0→97:3) to give 2-(cyclopropylmethyl-propyl-amino)-5-trifluoromethyl-benzaldehyde (1.7 g). MS (m/z): 286 [M+H]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906517B2
Source datasetuspto-grants-2011_03
ORD IDord-04a5abb2096c4251aa38342541870e2d
Source noteuspto-grants-2011_03