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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854952Generated: October 29, 2026

Formaldehyde → 2-Hydroxy-3,4,6-trimethylbenzaldehyde

https://huagongshe.com/reaction/854952

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
Reactant2,3,5-TrimethylphenolHCID 12769—
ReactantMagnesium ChlorideHCID 5360315—
SolventAcetonitrileHCID 6342—
Product2-Hydroxy-3,4,6-trimethylbenzaldehydeHCID 11321146—

Reaction Steps

To a solution of 2,3,5-trimethylphenol (11.2 g, 82.0 mmoles) in 400 mL of acetonitrile was added paraformaldehyde (17.2 g, 574 mmoles), anhydrous MgCl2 (11.7 g, 123 mmoles), and TEA (43 mL 31 g, 308 mmoles). The mixture was refluxed for 6 h with stirring. After cooling, the mixture was partially concentrated, water added, and the mixture acidified with dilute aqueous HCl. The mixture was extracted with three times with Et2O, the combined organic extracts washed with brine, dried over Na2SO4, filtered, and concentrated. Chromatography of the residue over silica gel using DCM as eluent gave 6-hydroxy-2,4,5-trimethylbenzaldehyde, 8.8 g, as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259266B2
Source datasetuspto-grants-2007_08
ORD IDord-9108c67313a9448182da326457150ba3
Source noteuspto-grants-2007_08