Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Ethyl formate | HCID 8025 | — |
| Reactant | Ethyl fluoroacetate | HCID 9988 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 53924449 | HCID 53924449 | — |
Reaction Steps
NaH (60% suspension in mineral oil, 15.6 g, 0.39 mole) was washed with and suspended in ether (300 mL). To this suspension, ethyl formate (29.1 mL, 0.36 mole, 1.2 eq) was added and the mixture was cooled in an ice bath. Ethyl fluoroacetate (29.0 mL, 0.3 mole) was added slowly over 1 hour. After 2 hours the ice bath was removed and the reaction was stirred for another hour. After evaporation of the solvent, the residue was redissolved in 350 mL of dry DMF and cooled in an ice bath, and ethyl iodide (48 mL, 0.6 mole) was added dropwise. The solution was allowed to warm to room temperature and stirred overnight, then quenched with saturated aqueous solution of NH4Cl (100 mL). The mixture was diluted with ether and extracted with water. The separated ether layer was washed with sodium thiosulfate, brine and dried over MgSO4. After concentration under vacuum, the residue was distilled to give ethyl 3-ethoxy-2-fluoroacrylate (12, R9 =ethyl, 73°-85° C./14 mmHg) as a colorless oil. 1H NMR (300 MHz, CDCl3): δ1.35 (t, 3H), 1.39 (t, 3H), 4.10 (q, 2H), 4.30 (q, 2H), 6.95 (d, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05693813 |
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| Source dataset | uspto-grants-1997_12 |
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| ORD ID | ord-899c74c426ee4f16bb5df7b0e38e83c3 |
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| Source note | uspto-grants-1997_12 |
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