HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767413Generated: October 30, 2026
Ethyl bromoacetate → (1,3-benzodioxol-5-yloxy)acetic acid
https://huagongshe.com/reaction/1767413
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sesamol | HCID 68289 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | (1,3-benzodioxol-5-yloxy)acetic acid | HCID 1531512 | 11.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USRE039707E1 |
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| Source dataset | uspto-grants-2007_06 |
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| ORD ID | ord-32ae8cf0e49b4c8786aa1717997b02a3 |
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| Source note | uspto-grants-2007_06 |
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