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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1791060Generated: November 4, 2026

Water → 5-Acetyl-2-{[2-(iodomethyl)-2-propenyl]oxy}benzaldehyde

https://huagongshe.com/reaction/1791060

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium IodideHCID 5238—
Reactant5-Acetyl-2-{[2-(chloromethyl)-2-propenyl]oxy}benzaldehydeHCID 22042271—
SolventAcetoneHCID 180—
Product5-Acetyl-2-{[2-(iodomethyl)-2-propenyl]oxy}benzaldehydeHCID 22042281100.1%

Reaction Steps

531 mg (3.54 mmol) of sodium iodide are added to 894 mg (3.54 mmol) of 5-acetyl-2-{[2-(chloromethyl)-2-propenyl]oxy}benzaldehyde in solution in 10 ml of distilled acetone. The medium is brought to reflux and is stirred for 5 hours. Water is added and then the solution is concentrated. After the addition of water and dichloromethane, the phases are separated by settling and then the aqueous phase is extracted with dichloromethane. The combined organic phases are washed, dried and then concentrated under vacuum to give 1.22 g (100%) of 5-acetyl-2-{[2-(iodomethyl)-2-propenyl]oxy}benzaldehyde in the form of a white solid which turns yellow in air; 1H NMR (300 MHz, CDCl3): 10.46 (s, 1H), 8.34 (d, J=2.4 Hz, 1H), 8.15 (dd, J=2.4 Hz and 8.7 Hz, 1H), 7.08 (d, J=8.7 Hz, 1H), 5.52 and 5.32 (2s, 2H), 4.86 (s, 2H), 4.01 (s, 2H), 2.54 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07071340B2
Source datasetuspto-grants-2006_07
ORD IDord-74898563749d45e290e940e012a4e69f
Source noteuspto-grants-2006_07