Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1717664Generated: October 31, 2026

Formaldehyde → 2-Hydroxy-4-iodobenzaldehyde

https://huagongshe.com/reaction/1717664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantTriethylamineHCID 8471—
Reactant3-IodophenolHCID 12272—
ReactantAmmonium ChlorideHCID 25517—
ReactantMagnesium ChlorideHCID 5360315—
SolventAcetonitrileHCID 6342—
Product2-Hydroxy-4-iodobenzaldehydeHCID 18351513160.1%

Reaction Steps

To a solution of 3-iodophenol (3.00 g, 13.6 mmol) in acetonitrile (50 mL) was added magnesium chloride (3.89 g, 40.9 mmol), triethylamine (7.6 mL, 55 mmol), and paraformaldehyde (1.64 g, 55 mmol). The reaction mixture was refluxed overnight, then neutralized with saturated aqueous ammonium chloride. The resultant red precipitate was removed by filtration, and the filtrate was extracted with ethyl acetate. The precipitate was dissolved in methanol and added to the combined organic extracts, which were then dried over magnesium sulfate. The solvent was removed under reduced pressure to provide an orange solid (5.4 g) as the crude product. This material was used in the subsequent step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803956B2
Source datasetuspto-grants-2010_09
ORD IDord-564595b1e0fe4de1887cbe30f638a6c4
Source noteuspto-grants-2010_09