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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 736779Generated: October 29, 2026

Methyl iodide → Methyl 3-methyl-4-oxooxane-3-carboxylate

https://huagongshe.com/reaction/736779

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 4-oxooxane-3-carboxylateHCID 14666555—
Reactantmethyl 4-hydroxy-5,6-dihydro-2H-pyran-3-carboxylateHCID 68541653—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductMethyl 3-methyl-4-oxooxane-3-carboxylateHCID 6881928461%

Reaction Steps

Methyl 4-oxo-tetrahydro-2H-pyran-3-carboxylate and methyl 4-hydroxy-5,6-dihydro-2H-pyran-3-carboxylate (13.5 g, 85.5 mmol) were dissolved in DMF (70 mL). Sodium hydride (60%, 3.6 g, 1.05 eq) was added at 0° C. After 10 min, iodomethane (6.7 mL, 1.25 eq) was added. The reaction was stirred overnight, diluted with ethyl acetate (200 mL), and washed with water (5×100 mL). The aqueous layer was re-extracted with ethyl acetate. The combined organic layers were washed with brine, dried over MgSO4, and concentrated. The residue was purified by chromatography on silica gel eluting with 20% ethyl acetate/hexane to yield 8.2 g (61%) of methyl 3-methyl-4-oxo-tetrahydro-2H-pyran-3-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07595327B2
Source datasetuspto-grants-2009_09
ORD IDord-4436b5a6cbe04081ab88f5302356c23f
Source noteuspto-grants-2009_09