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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzoic Acid | HCID 243 | — |
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Methyl 3,5-diallyloxy-2-ethylphenylacetate | HCID 23116370 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | Methyl 3,5-diallyloxy-2-benzoyl-6-ethylphenylacetate | HCID 86610520 | 56.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07538224B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-0466909da58e4e95b2d42e6f404b538c |
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| Source note | uspto-grants-2009_05 |
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