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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1938825Generated: November 2, 2026

Iodoethane → HCID 53924449, compound

https://huagongshe.com/reaction/1938825

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantEthyl formateHCID 8025—
ReactantEthyl fluoroacetateHCID 9988—
ReactantSodium hydrideHCID 24758—
SolventDiethyl EtherHCID 3283—
ProductHCID 53924449HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05693813
Source datasetuspto-grants-1997_12
ORD IDord-899c74c426ee4f16bb5df7b0e38e83c3
Source noteuspto-grants-1997_12