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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1815519Generated: October 29, 2026

Iodoethane → HCID 22498573, compound

https://huagongshe.com/reaction/1815519

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 NaHCO3 (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 numberUS06878700B1
Source datasetuspto-grants-2005_04
ORD IDord-b7b2004d9eed490f8cbfe4d428614dad
Source noteuspto-grants-2005_04