Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1992660Generated: October 31, 2026

Methyl iodide → Methyl 3-(2,4-difluorophenyl)acrylate

https://huagongshe.com/reaction/1992660

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant3-(2,4-Difluorophenyl)acrylic AcidHCID 603502—
SolventDimethylformamideHCID 6228—
ProductMethyl 3-(2,4-difluorophenyl)acrylateHCID 1527647377%

Reaction Steps

To a solution of 2,4-difluorocinnamic acid (20 g, 135 mmol) in N,N-dimethylformamide (500 mL) at room temperature under dry nitrogen was added potassium carbonate (90 g, 675 mmol) then iodomethane (21 mL, 337.5 mmol). The resulting mixture was stirred at room temperature under dry nitrogen for 7 hours before being quenched by the addition of water (1 L) and extracted with diethyl ether (3×200 mL). The combined organic extracts were dried over magnesium sulfate, filtered, and concentrated in vacuo. The residue was purified by an automated flash column chromatography system (CombiFlash® Separation System Sg 100c by Isco) using a pre-packed column (Redisep™ Disposable Columns for Flash Chromatography by Isco, 120 g column) eluting with 2% ethyl acetate in pentane increasing polarity in a linear gradient to 10% ethyl acetate in pentane over 1 hour to afford the title compound as a white solid (20.5 g, 77%). 1H NMR (400 MHz, CDCl3) δH 3.80 (3H, s), 6.50 (1H, d), 6.85 (1H, m), 7.50 (1H, m), 7.75 (1H, d); LRMS (APCI) 216 [MNH4+], 199 [MH+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07649002B2
Source datasetuspto-grants-2010_01
ORD IDord-b49b375c995440309c4dab543b6ecb0f
Source noteuspto-grants-2010_01