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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1697201Generated: October 29, 2026

Ethyl acetate hexane → 1-(3-(Methoxymethoxy)-6-neopentylpyridin-2-yl)ethanone

https://huagongshe.com/reaction/1697201

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl acetate hexaneHCID 21226206—
Reactant3-(Methoxymethoxy)-6-neopentylpicolinonitrileHCID 67165673—
ReactantHCID 178418332HCID 178418332—
SolventTetrahydrofuranHCID 8028—
Product1-(3-(Methoxymethoxy)-6-neopentylpyridin-2-yl)ethanoneHCID 5751584343%

Reaction Conditions

Temperature0 °C

Reaction Steps

3-(Methoxymethoxy)-6-neopentylpicolinonitrile (8.3 g, 35 mmol) was dissolved in THF (125 mL). The solution was cooled to 0° C. and methylmagnesium chloride (24 ml, 71 mmol) (3.0 M in Et2O) was added. The reaction mixture stirred for 2 h at rt under N2 then quenched with saturated NH4Cl (50 mL) and extracted with EtOAc (3×50 mL). The organic layer was dried over MgSO4 and evaporated to give the crude product as a yellow oil. Purification of the crude residue by ISCO (40 g SiO2, O-40% EtOAc/Hexane) gave 1-(3-(methoxymethoxy)-6-neopentylpyridin-2-yl)ethanone (3.8 g, 43% yield) as a clear, light orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163909B2
Source datasetuspto-grants-2012_04
ORD IDord-c10158cb40194f35aa9492d5bd2f2824
Source noteuspto-grants-2012_04