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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2091178Generated: November 2, 2026

Acetic Acid → 5-Methoxy-3-methylbenzofuran

https://huagongshe.com/reaction/2091178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAcetic AnhydrideHCID 7918—
ReactantAcetic acid, 2-(2-acetyl-4-methoxyphenoxy)-HCID 13156994—
SolventWaterHCID 962—
Product5-Methoxy-3-methylbenzofuranHCID 1315699881.1%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of (2-acetyl-4-methoxyphenoxy)acetic acid (10.0 g) synthesized above, acetic anhydride (18.3 g) and acetic acid (100 mL) was stirred at 110° C. for 5 hr, poured into water, and the mixture was extracted with ethyl acetate. The extract was washed with saturated aqueous sodium hydrogen carbonate solution and saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (5% ethyl acetate/hexane) to give the title object compound (5.87 g, 81%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436043B2
Source datasetuspto-grants-2013_05
ORD IDord-741101901d7541238fe4c451fc6c11a5
Source noteuspto-grants-2013_05