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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854922Generated: October 30, 2026

Formaldehyde → 2-Hydroxy-3,5-dimethylbenzaldehyde

https://huagongshe.com/reaction/854922

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
Reactant2,4-DimethylphenolHCID 7771—
ReactantHexamethylphosphoramideHCID 12679—
CatalystHCID 178418443HCID 178418443—
SolventTolueneHCID 1140—
Product2-Hydroxy-3,5-dimethylbenzaldehydeHCID 477024559%

Reaction Steps

To a solution of 2,4-dimethylphenol (24.9 g, 204 mmole) in anhydrous toluene (75 mL) at 0° C. was added HMPA (35 mL) and then a solution of ethylmagnesium bromide (61 mL-3 M in ethyl ether, 0.183 mmole), keeping the temperature <10° C. Then paraformaldehyde (13 g, 0.43 mole) was added and the cooling was removed. The ethyl ether was removed by distillation and the mixture was refluxed. The mixture was quenched with 10% HCl and EtOAc was added. The EtOAc solution was washed twice with H2O, twice with aqueous NH4Cl, dried over Na2SO4 and concentrated in vacuo. Purification by silica chromatography (98:2 hexanes:EtOAc) gave 17.9 g (59% yield) of the product as a yellow oil: ESHRMS m/z 147.0619 (M−H, C9H9O2, Calc'd 147.0603).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259266B2
Source datasetuspto-grants-2007_08
ORD IDord-2be9918480ce4678a5dcc36bf1bc4998
Source noteuspto-grants-2007_08