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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1363481Generated: October 30, 2026

Acetone → 4-(2-hydroxyethoxy)-3-methoxybenzaldehyde

https://huagongshe.com/reaction/1363481

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantVanillinHCID 1183—
Reactant2-BromoethanolHCID 10898—
ReactantPotassium CarbonateHCID 11430—
SolventEthanolHCID 702—
Product4-(2-hydroxyethoxy)-3-methoxybenzaldehydeHCID 315271240%

Reaction Steps

25.9 g (170 mmol) vanillin (Aldrich), 33.3 g (266 mmol) 2-bromoethanol (Aldrich), 35.2 g (255 mmol) potassium carbonate (Sigma-Aldrich), and 20 g molecular sieves (Aldrich) were combined in a 1 liter round bottom flask equipped with magnetic stirrer and nitrogen inlet. Acetone (600 ml) (Chromasolv for HPLC, >99.9%, Sigma-Aldrich) was added and the reaction mixture was refluxed for 16 hours using an external glycerol heating bath set to 65° C. The solids were filtered and the solvent was removed via rotary evaporation to yield a yellow oil. White crystals were obtained by recrystallization in ethyl alcohol at −20° C. (40% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07884228B1
Source datasetuspto-grants-2011_02
ORD IDord-5af7dc44547d4f008b8395d19d2bdc30
Source noteuspto-grants-2011_02