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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2236569Generated: October 31, 2026

3,4-Dihydroxybenzaldehyde → 3-Hydroxy-4-(2-methoxyethoxy)benzaldehyde

https://huagongshe.com/reaction/2236569

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-DihydroxybenzaldehydeHCID 8768—
ReactantSodium CarbonateHCID 10340—
Reactant2-Bromoethyl methyl etherHCID 80972—
SolventDimethylformamideHCID 6228—
Product3-Hydroxy-4-(2-methoxyethoxy)benzaldehydeHCID 4262551930%

Reaction Steps

An amount of 3,4-dihydroxybenzaldehyde (5.0 g, 36.2 mmol) in 20 mL of N,N′-dimethylformamide is added 2-bromoethyl methyl ether (3.4 mL, 36.2 mmol), and sodium carbonate (5.0 g, 72.4 mmol). The reaction mixture is stirred at room temperature for 3 days. After removal solids by filtration, the solution is subsequently evaporated under high-pressure vacuum to dark brown liquid. The residue is added water and acidified with 12 N HCl solution to pH˜2, then extracted 4×100 mL of EtOAc. The combined organic layer is washed with brine, dried over Mg2SO4, stirred in darko, filtered and evaporated to give yellow liquid. Purification is performed by column chromatography over silica gel using 40% EtOAc/Hex as eluent to give 2.13 g of colorless solid: mp 74-75° C.; MS (ESI) m/z 195.1 (M+H)−1

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07713994B2
Source datasetuspto-grants-2010_05
ORD IDord-1dc04bc8738441ccba5d05bf4c008aa3
Source noteuspto-grants-2010_05