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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1497690Generated: October 26, 2026

Triethylamine → (Z)-Ethyl 3-(dimethylamino)-2-(3-fluoropicolinoyl)acrylate

https://huagongshe.com/reaction/1497690

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl trans-3-dimethylaminoacrylateHCID 5369162—
Reactant3-Fluoropyridine-2-carbonyl chlorideHCID 86102307—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product(Z)-Ethyl 3-(dimethylamino)-2-(3-fluoropicolinoyl)acrylateHCID 8672544516.6%

Reaction Conditions

Temperature83 °C

Reaction Steps

To a light yellow solution of (E)-ethyl 3-(dimethylamino)acrylate (5.15 g, 36.0 mmol) in toluene (50 mL) was added triethylamine (3.64 g, 5.02 mL, 36.0 mmol) at room temperature. To this, a dark brown suspension of 3-fluoropicolinoyl chloride (30) (4.79 g, 30 mmol) in toluene (50 mL, heated to dissolve, but not dissolved completely) was added in one portion using a funnel. Then, the resulting dark brown solution was heated to 83° C. and stirred for 1.5 h at this temperature. During this period, it turned to a dark brown solution and TLC analysis indicated the presence of a new spot. Then, the heating was stopped and the dark brown mixture was diluted with ethyl acetate (200 mL) and the brown solution was washed with water, brine solution, and dried over anhydrous MgSO4. Filtration and concentration gave the crude brown mixture which was purified using ISCO (120 g) column chromatography, eluting with ethyl acetate in hexanes (0 to 100%) and then 5 to 20% methanol in dichloromethane. The desired fractions were combined and the solvent was removed under vacuum to obtain the (Z)-ethyl 3-(dimethylamino)-2-(3-fluoropicolinoyl)acrylate (31) (1.33 g, 15% yield) as a dark brown paste.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199987B2
Source datasetuspto-grants-2015_12
ORD IDord-cf5c752ae14e40ab8d18cc68d78a5194
Source noteuspto-grants-2015_12