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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 499869Generated: October 25, 2026

Acetic Acid → Methyl 2-acetyl-3,5-diallyloxyphenylacetate

https://huagongshe.com/reaction/499869

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantSodium BicarbonateHCID 516892—
ReactantMethyl 3,5-diallyloxyphenylacetateHCID 23116191—
SolventTrifluoroacetic acidHCID 6422—
ProductMethyl 2-acetyl-3,5-diallyloxyphenylacetateHCID 6842177670.4%

Reaction Conditions

Temperature4 °C

Reaction Steps

Methyl 3,5-diallyloxyphenylacetate (40 g, 0.14 mol) obtained in Example 5, Step 1 was dissolved in trifluoroacetic acid (0.15 L). After the solution was cooled to 4° C., acetic acid (9.5 mL, 0.17 mol) and trifluoroacetic anhydride (40 mL, 0.28 mol) were added thereto, followed by stirring at 4° C. for 3.5 hours. The reaction mixture was gradually added to a saturated aqueous solution of sodium hydrogencarbonate for neutralization, followed by extraction with ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (ethyl acetate/hexane=1/20-1/6) to obtain methyl 2-acetyl-3,5-diallyloxyphenylacetate (30 g, 65%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07767693B2
Source datasetuspto-grants-2010_08
ORD IDord-7e45bf1e3f5e448c849e1aa7fa713d8f
Source noteuspto-grants-2010_08