HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2076620Generated: November 1, 2026
Water → Methyl (3-methoxy-4-{[(trifluoromethyl)sulfonyl]oxy}phenyl)acetate
https://huagongshe.com/reaction/2076620
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Trifluoromethanesulfonic acid | HCID 62406 | — |
| Reactant | Methyl 4-hydroxy-3-methoxyphenylacetate | HCID 85214 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl (3-methoxy-4-{[(trifluoromethyl)sulfonyl]oxy}phenyl)acetate | HCID 86617406 | 99.9% |
Reaction Steps
Pyridine (2.10 ml, 25.9 mmol), anhydrous trifluoromethanesulfonic acid (1.61 ml, 9.53 mmol) and 4-dimethylaminopyridine (30 mg, 0.25 mmol) were added to a solution of methyl (4-hydroxy-3-methoxyphenyl)acetate (1.70 g, 8.66 mmol) in methylene chloride (20 ml) and the mixture was stirred under ice-cooling for 10 minutes and then stirred at room temperature for 20 minutes. After the reaction mixture was poured into water and the mixture was extracted with ethyl acetate, the organic layer was successively washed with water (twice) and a saturated aqueous NaCl solution and dried with anhydrous sodium sulfate. The residue obtained by removing the solvent under reduced pressure was purified by silica gel column chromatography (eluting solvent: n-hexane/ethyl acetate=2/1) to give methyl (3-methoxy-4-{[(trifluoromethyl)sulfonyl]oxy}phenyl)acetate (2.84 g, yield: 99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07923573B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-72801ca5016047b8bc0b45013c1383e6 |
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| Source note | uspto-grants-2011_04 |
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