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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 984500Generated: October 30, 2026

Iodoethane → HCID 22498573, compound

https://huagongshe.com/reaction/984500

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-(Furan-2-yl)prop-2-enoic acidHCID 316259—
SolventAcetonitrileHCID 6342—
ProductHCID 22498573HCID 22498573—

Reaction Conditions

Temperature60 °C

Reaction Steps

Ethyl iodide (64 mL, 0.796 mol) was added to furylacrylic acid (100 g, 0.724 mol), diisopropylethyl amine (140 mL, 0.796 mmol), in acetonitrile (1100 mL), and the mixture was heated to 60° C. After 18 h, the dark solution was cooled to room temperature and concentrated in vacuo. The resulting brown sludge was diluted with Et2O (500 mL), washed with 1 N aqueous HCl (2×250 mL), washed with 0.2 N aqueous NaOH (2×250 mL), washed with saturated aqueous NaH.CO3 (1×250 ML), dried (MgSO4), filtered, and concentrated to a black oil (114 g, 95%). 1H NMR (DMSO-d6, 300 MHz) δ 7.84 (d, J=1.7 Hz, 1H), 7.46 (d, J=15.6 Hz, 1H), 6.97 (d, J=3.4 Hz, 1H), 6.33 (dd, J=3.4 Hz, J=1.7 Hz, 1H), 6.22 (d, J=15.9 Hz, 1H), 4.17 (q, J=7.1 Hz, 2H), 1.24 (t, J=7.1 Hz, 3H); MS (APCI) m/z 167 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06867203B2
Source datasetuspto-grants-2005_03
ORD IDord-ff54e552bb4741da9bbac62949e605dc
Source noteuspto-grants-2005_03