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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1057183Generated: November 3, 2026

N-Iodosuccinimide → (E)-ethyl 3-(4-iodophenyl)acrylate

https://huagongshe.com/reaction/1057183

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
Reactant4-(E-3-Ethoxy-3-oxo-1-propen-1-yl)benzeneboronic acidHCID 5942507—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product(E)-ethyl 3-(4-iodophenyl)acrylateHCID 2110727686.1%

Reaction Steps

N-Iodosuccinimide (2.5 g, 11 mmol) was added to a suspension of 4-(E-3-ethoxy-3-oxo-1-propen-1-yl)phenylboronic acid (2.2 g, 10 mmol) in CH3CN (50 mL) at room temperature. The reaction was covered with foil, stirred for 26 h, and then diluted with EtOAc. The resulting mixture was washed with water (2×100 mL), washed with sodium thiosulfate (100 mL), dried (MgSO4), filtered, and concentrated. The crude material was purified by silica gel chromatography (0-50% EtOAc in hexanes) to give 2.6 g of (E)-ethyl 3-(4-iodophenyl)acrylate as a yellow oil. 1H NMR (400 MHz, DMSO-d6): δ 7.79 (d, 2H), 7.60 (d, 1H), 7.53 (d, 2H), 6.68 (d, 1H), 4.19 (q, 2H), 1.26 (t, 3H); LCMS: 303 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09399646B2
Source datasetuspto-grants-2016_07
ORD IDord-80fed62a93c8441ca1baaa323d5d139b
Source noteuspto-grants-2016_07