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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443350Generated: October 27, 2026

Formaldehyde → 2-Hydroxy-4-iodobenzaldehyde

https://huagongshe.com/reaction/1443350

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 numberUS07659412B2
Source datasetuspto-grants-2010_02
ORD IDord-35bbc710d6b94f938ab960e60f671581
Source noteuspto-grants-2010_02