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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Reactant | 3-(Methoxymethoxy)-6-neopentylpicolinonitrile | HCID 67165673 | — |
| Reactant | HCID 178418332 | HCID 178418332 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(3-(Methoxymethoxy)-6-neopentylpyridin-2-yl)ethanone | HCID 57515843 | 43% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08163909B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-c10158cb40194f35aa9492d5bd2f2824 |
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| Source note | uspto-grants-2012_04 |
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