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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 617398Generated: October 30, 2026

Water → Ethyl alpha-methoxy-2-(tetrahydropyran-2-yloxymethyl)phenylacetate

https://huagongshe.com/reaction/617398

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantEthyl alpha-hydroxy-2-(tetrahydropyran-2-yloxymethyl)phenylacetateHCID 18357802—
SolventDimethylformamideHCID 6228—
ProductEthyl alpha-methoxy-2-(tetrahydropyran-2-yloxymethyl)phenylacetateHCID 1835780395.5%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05948819
Source datasetuspto-grants-1999_09
ORD IDord-f54d4ca94e5742bd872ae4ae97f598ae
Source noteuspto-grants-1999_09