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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1597857Generated: November 1, 2026

3-Hydroxybenzaldehyde → Ethyl 2-(3-formylphenoxy)acetate

https://huagongshe.com/reaction/1597857

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-HydroxybenzaldehydeHCID 101—
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
SolventAcetoneHCID 180—
ProductEthyl 2-(3-formylphenoxy)acetateHCID 1494377—

Reaction Steps

To a mixture of 3-hydroxybenzaldehyde (5.17 g, 42.34 mmol), K2 CO3 (5.85 g) and acetone (50 ml) was added ethyl bromoacetate (5.2 ml). The reaction mixture was stirred at room temperature overnight, additional K2CO3 (1 equivalent) was added, the mixture was stirred for one hour, then additional ethyl bromoacetate (0.5 equivalents) was added and the mixture was stirred at room temperature until the reaction was complete. The reaction mixture was filtered, water was added to the filtrate and the solvent was removed. The residue was dissolved in ether, extracted with 1M NaOH (2×100 ml), and the ether layer was dried over MgSO4 and stripped to afford, as a liquid, 7.89 g of 3-(ethoxycarbonylmethoxy) benzaldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05736548
Source datasetuspto-grants-1998_04
ORD IDord-dab5f8db7da242c284b1cb35a470c754
Source noteuspto-grants-1998_04