Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 468693Generated: October 30, 2026

Water → 4-(Difluoromethoxy)-3,5-dimethoxybenzaldehyde

https://huagongshe.com/reaction/468693

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl chlorodifluoroacetateHCID 73935—
Reactant4-Hydroxy-3,4-dimethoxybenzaldehydeHCID 86650355—
SolventDimethylformamideHCID 6228—
Product4-(Difluoromethoxy)-3,5-dimethoxybenzaldehydeHCID 71059839%

Reaction Conditions

Temperature67.5 °C

Reaction Steps

Methyl chlorodifluoroacetate (0.58 mL, 5.5 mmol) was added to a suspension of 4-hydroxy-3,4-dimethoxybenzaldehyde (0.50 g, 2.7 mmol) and potassium carbonate (0.76 g, 5.5 mol) in DMF (5.0 mL). The suspension was heated to 65-70° C. for 16 h and the suspension was diluted with water. The aqueous phase was extracted with EtOAc and the combined organic fractions were washed with saturated aqueous NaHCO3, water, brine, dried and concentrated. The crude product was recrystallised from EtOAc/petrol providing 4-(difluoromethoxy)-3,5-dimethoxybenzaldehyde (0.25 g, 39%) as a colourless crystalline solid; mp 113-115° C.; δH (400 MHz, CDCl3) 3.95 (s, 6H, OCH3), 6.65 (t, J=74 Hz, 1H, OCHF2), 7.15 (s, 2H, H2, H6), 9.91 (s, 1H, CHO); δC (100 MHz, CDCl3) δ6.5, 106.3, 116.2 (t, J=256 Hz), 134.1, 153.5, 190.8; νmax 831, 1048, 1099, 1330, 1600, 1699, 2854 cm−1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08624056B2
Source datasetuspto-grants-2014_01
ORD IDord-82ff59ce80314f98b1f58463600fd8da
Source noteuspto-grants-2014_01