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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1700247Generated: November 1, 2026

Ethyl bromoacetate → (1,3-benzodioxol-5-yloxy)acetic acid

https://huagongshe.com/reaction/1700247

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
ReactantSesamolHCID 68289—
SolventAcetoneHCID 180—
Product(1,3-benzodioxol-5-yloxy)acetic acidHCID 153151211.5%

Reaction Steps

The mixture of sesamol (270 mg, 2.0 mmol), potassium carbonate (910 mg, 6.6 mmol), ethyl bromoacetate (2.55 ml, 22.9 mmol) and acetone (25 ml) was refluxed for 21 h. After cooling, the mixture was filtered to remove potassium carbonate. The filtrate was concentrated under reduced pressure. To this residue, 20 ml dioxane and 14 ml 5% sodium hydroxide solution were added. After the uiixture was stirred at room temperature overnight, it was acidified with concentrated hydrochloric acid to pH 2, and then extracted three times with ethyl acetate (20 ml each). Organic phases were combined, washed with water and brine, dried over magnesium sulfate, filtered, and then evaporated in vacuo. The residue was recrystallized from chloroform and acetone to give 45 mg 3,4-methylenedioxyphenoxyacetic acid as white crystals, mp 149-151 ° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06350756B1
Source datasetuspto-grants-2002_02
ORD IDord-eece8e3ec94043cf9e52ed4b152a5068
Source noteuspto-grants-2002_02