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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1647165Generated: November 2, 2026

Methyl iodide → HCID 19926461, compound

https://huagongshe.com/reaction/1647165

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium HydroxideHCID 14797—
Reactant3-(3-Hydroxypropoxy)-2-methyl-4H-pyran-4-oneHCID 10464989—
ProductHCID 19926461HCID 1992646120.6%

Reaction Steps

A mixture of 3-(3-hydroxy-1-propoxy)-2-methyl-4-pyrone {1.4 g, 7.6 mmol), 85% KOH (0.55 g, 8.4 mmol) and methyliodide (11 g, 76 mmol) was stirred at room temperature for one day. The red solution was partitioned between methylene chloride and half saturated aqueous ammoniumchloride solution. The organic phase was washed with water, dried over Na2SO4 and evaporated. The residue was purified by chromatography on silica gel with methanol/methylene chloride (3:97) as eluent. Removing the eluent by film evaporation afforded 0.31 g (20%) of the desired product as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05430042
Source datasetuspto-grants-1995_07
ORD IDord-9cc9654cd47f495994330c1bdeb041e4
Source noteuspto-grants-1995_07