HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 499883Generated: October 30, 2026
Isovanillic Acid → HCID 86610524, compound
https://huagongshe.com/reaction/499883
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isovanillic Acid | HCID 12575 | — |
| Reactant | HCID 45093151 | HCID 45093151 | — |
| Solvent | Boron trifluoride etherate | HCID 8000 | — |
| Product | HCID 86610524 | HCID 86610524 | 65% |
Reaction Steps
Methyl 2-ethyl-3,5-dihydroxyphenylacetate (2.0 g, 9.7 mmol) obtained in Example 7, Step 2 was suspended in boron trifluoride diethyl etherate (40 mL), and 3-hydroxy-4-methoxybenzoic acid (1.7 g, 11 mmol) was added thereto, followed by stirring at 80° C. for 5 hours. After cooling to room temperature, the reaction mixture was added dropwise to ice-cold water, and the resulting mixture was extracted with ethyl acetate. The organic layer was washed successively with a saturated aqueous solution of sodium hydrogencarbonate and 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=1/4-9/1) to obtain methyl 2-ethyl-3,5-dihydroxy-6-(3-hydroxy-4-methoxy-benzoyl)phenylacetate (2.2 g, 65%).
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-02efee12e6664601a7050132b12e834b |
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| Source note | uspto-grants-2010_08 |
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