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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 495182Generated: October 29, 2026

Benzoic Acid → Methyl 3,5-diallyloxy-2-benzoyl-6-ethylphenylacetate

https://huagongshe.com/reaction/495182

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoic AcidHCID 243—
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantSodium BicarbonateHCID 516892—
ReactantMethyl 3,5-diallyloxy-2-ethylphenylacetateHCID 23116370—
SolventTrifluoroacetic acidHCID 6422—
ProductMethyl 3,5-diallyloxy-2-benzoyl-6-ethylphenylacetateHCID 8661052056.6%

Reaction Conditions

Temperature4 °C

Reaction Steps

Methyl 3,5-diallyloxy-2-ethylphenylacetate (0.31 g, 1.3 mmol) obtained in Example 5, Step 3 was dissolved in trifluoroacetic acid (2.0 mL). After the solution was cooled to 4° C., benzoic acid (0.40 g, 3.3 mmol) and trifluoroacetic anhydride (1.0 mL) were added thereto, followed by stirring for 18 hours, while the temperature of the reaction mixture was raised to room temperature. 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 dried over anhydrous sodium sulfate and then concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (ethyl acetate/hexane=1/9-1/4) to obtain methyl 3,5-diallyloxy-2-benzoyl-6-ethylphenylacetate (0.29 g, 55%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07538224B2
Source datasetuspto-grants-2009_05
ORD IDord-0466909da58e4e95b2d42e6f404b538c
Source noteuspto-grants-2009_05