HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 499882Generated: October 30, 2026
4-Hydroxybenzoic Acid → Methyl 3,5-diallyloxy-2-ethyl-6-(4-hydroxybenzoyl)phenylacetate
https://huagongshe.com/reaction/499882
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Hydroxybenzoic Acid | HCID 135 | — |
| 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-ethyl-6-(4-hydroxybenzoyl)phenylacetate | HCID 86610523 | 62% |
Reaction Steps
Methyl 3,5-diallyloxy-2-ethylphenylacetate (1.0 g, 3.3 mmol) obtained in Example 5, Step 3 was dissolved in trifluoroacetic acid (9.0 mL), and 4-hydroxybenzoic acid (1.4 g, 10 mmol) and trifluoroacetic anhydride (1.2 mL) were added thereto, followed by stirring at room temperature for 20 hours. To the mixture were further added 4-hydroxybenzoic acid (0.92 g, 6.6 mmol) and trifluoroacetic anhydride (1.4 mL), followed by stirring for 6 hours. The reaction mixture was added dropwise to a saturated aqueous solution of sodium hydrogencarbonate (0.10 L), and the resulting mixture was extracted with ethyl acetate (50 mL×4). The organic layer was dried over anhydrous sodium sulfate and then concentrated under reduced pressure. The resulting residue was dissolved in a 7 mol/L solution of ammonia in methanol (100 mL), followed by stirring at room temperature for 1 day. After the reaction mixture was concentrated under reduced pressure, 3 mol/L hydrochloric acid (40 mL) was added thereto, followed by extraction with ethyl acetate (50 mL×3). The organic layer was washed with water, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (ethyl acetate/hexane=1/10-1/2) to obtain methyl 3,5-diallyloxy-2-ethyl-6-(4-hydroxybenzoyl)phenylacetate (0.84 g, 57%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07767693B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-03d10934973c4399a618736aa88d7646 |
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| Source note | uspto-grants-2010_08 |
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