HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1962549Generated: October 29, 2026
Ethyl cyanoacetate → Ethyl 2-cyano-4-(2,6-difluorophenyl)-4-oxobutanoate
https://huagongshe.com/reaction/1962549
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl cyanoacetate | HCID 7764 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2,6-Difluorophenacyl bromide | HCID 2778263 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 2-cyano-4-(2,6-difluorophenyl)-4-oxobutanoate | HCID 66974573 | 81% |
Reaction Steps
To a solution of ethyl cyanoacetate (7.24 g) and diisopropylethylamine (19.9 g) in tetrahydrofuran (30 mL) was added dropwise a solution of 2-bromo-1-(2,6-difluorophenyl)ethanone (15.16 g) in tetrahydrofuran (15 mL) at 10-15° C. The mixture was stirred at room temperature for 12 hr. The reaction mixture was filtered, and the obtained filtrate was concentrated under reduced pressure. The residue was dissolved in ethyl acetate, washed successively with water, 1 mol/L hydrochloric acid and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate=4:1→3:2) to give the title compound as a pale-green oil (yield 13.8 g, 81%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08415368B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-4118e1fc0a794c47be5dabe18c154270 |
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| Source note | uspto-grants-2013_04 |
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