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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-(2,4-Difluorophenyl)acrylic Acid | HCID 603502 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 3-(2,4-difluorophenyl)acrylate | HCID 15276473 | 77% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07649002B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-b49b375c995440309c4dab543b6ecb0f |
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| Source note | uspto-grants-2010_01 |
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