HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 48156Generated: October 25, 2026
Methyl iodide → Methyl 4-methoxyphenylacetate
https://huagongshe.com/reaction/48156
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Benzeneacetic acid, 4-hydroxy-, methyl ester | HCID 518900 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 4-methoxyphenylacetate | HCID 90266 | 83.1% |
Reaction Steps
A solution of methyl 4-hydroxyphenylacetate (25.0 g, 0.147 mol) in tetrahydrofuran (50 ml) was added dropwise to a stirred suspension of sodium hydride (4.45 g of an 80% dispersion in oil, 0.147 mol) in tetrahydrofuran (150 ml) and the mixture was stirred for 90 minutes. A solution of methyl iodide (20.9 g, 0.47 mol) in tetrahydrofuran (50 ml) was added dropwise and the mixture was stirred overnight at room temperature. The solvent was removed in vacuo, and the residue was partitioned between water and ethyl acetate. The organic extract was washed with brine, dried over anhydrous magnesium sulfate, filtered and the filtrate was evaporated in vacuo. The residue was purified by chromatography on silica gel, eluting with ethyl acetate:hexane 1:9, to give methyl 4-methoxyphenylacetate (22.0 g) as a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06703347B2 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-b18ace9b66fe460e9a61d18b4777618b |
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| Source note | uspto-grants-2004_03 |
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