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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 495105Generated: October 26, 2026

3-Hydroxybenzaldehyde → n-butyl (R)-2-(3-formylphenoxy)butyrate

https://huagongshe.com/reaction/495105

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-HydroxybenzaldehydeHCID 101—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant(S)-2-(Trifluoromethylsulfonyloxy)butanoic acid butyl esterHCID 25023368—
SolventAcetonitrileHCID 6342—
Productn-butyl (R)-2-(3-formylphenoxy)butyrateHCID 11846216—

Reaction Steps

Potassium carbonate (473 mg) was added to a solution of 3-hydroxybenzaldehyde (418 mg) in acetonitrile (10 mL). Subsequently, n-butyl (S)-2-trifluoromethanesulfonyloxybutyrate (1.0 g) was added to the mixture, followed by stirring at room temperature for 12 hours. Ethyl acetate was added to the reaction mixture, and the resultant mixture was washed sequentially with water and saturated brine, followed by drying over sodium sulfate anhydrate. The reaction mixture was filtered, and the filtrate was concentrated under reduced pressure. The residue was purified through silica gel column chromatography (hexane/ethyl acetate=4/1), to thereby yield 904 mg of a colorless, oily substance (99.9%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07538242B2
Source datasetuspto-grants-2009_05
ORD IDord-f3edbdc1d6d14417a7c6af4ca139b6e5
Source noteuspto-grants-2009_05