HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 428000Generated: October 30, 2026
Water → Ethyl alpha-methoxy-2-(tetrahydropyran-2-yloxymethyl)phenylacetate
https://huagongshe.com/reaction/428000
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl alpha-hydroxy-2-(tetrahydropyran-2-yloxymethyl)phenylacetate | HCID 18357802 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl alpha-methoxy-2-(tetrahydropyran-2-yloxymethyl)phenylacetate | HCID 18357803 | 95.5% |
Reaction Steps
Methyl iodide (20.25 g, 143 mmol) was added to a solution of ethyl α-hydroxy-2-(tetrahydropyran-2-yloxymethyl)phenylacetate (14.00 g, 47.6 mmol) in N,N-dimethylformamide (40 ml), and the mixture was stirred at 0° C. 60% oily sodium hydride (1.90 g, 47.5 mmol) was added thereto. After 30 minutes, water (100 ml) was added, and the mixture was extracted with ether and dried over anhydrous magnesium sulfate. The solvent was evaporated, and the residue was purified by column chromatography on silica gel (n-hexane/ ethyl acetate=4/1) to give the desired compound ethyl α-methoxy-2-(tetrahydropyran-2-yloxymethyl)phenylacetate (14.00 g, 95.5%) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06313150B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-406c2142f4254b1dac7c5304edb29bd7 |
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| Source note | uspto-grants-2001_11 |
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