HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 599615Generated: November 1, 2026
Hydrochloric Acid → Methyl methoxy-(4-methoxyphenyl)acetate
https://huagongshe.com/reaction/599615
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methyl 4-methoxyphenylacetate | HCID 90266 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | Iodo benzene diacetate | HCID 12217721 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl methoxy-(4-methoxyphenyl)acetate | HCID 10262525 | 15.6% |
Reaction Steps
A 28% solution of sodium methoxide in methanol (12.8 g) and iodobenzene diacetate (7.15 g) were added to a solution of methyl 4-methoxyphenylacetate (4.0 g) in methanol (60 mL), and the reaction solution was stirred at room temperature for five days. 1 N hydrochloric acid (67 ml) was added dropwise to the reaction solution under ice-cooling, and methanol was evaporated from the reaction solution under reduced pressure. Ethyl acetate was added to the remaining aqueous layer, and the organic layer was separated. The resulting organic layer was sequentially washed with a saturated sodium bicarbonate solution and brine, dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluting solvent: heptane-ethyl acetate system) to obtain 725 mg of the title compound. The property values of the compound are as follows.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07897632B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-e58ec8da09cd49e0aa1d169f65f5e68b |
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| Source note | uspto-grants-2011_03 |
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