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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1697202Generated: October 30, 2026

Isopropanol → 1-(3-Hydroxy-6-neopentylpyridin-2-yl)ethanone

https://huagongshe.com/reaction/1697202

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
ReactantTetrahydrofuranHCID 8028—
Reactant1-(3-(Methoxymethoxy)-6-neopentylpyridin-2-yl)ethanoneHCID 57515843—
SolventHydrochloric AcidHCID 313—
Product1-(3-Hydroxy-6-neopentylpyridin-2-yl)ethanoneHCID 5751584464%

Reaction Steps

A solution of 1-(3-(methoxymethoxy)-6-neopentylpyridin-2-yl)ethanone (3.75 g, 15 mmol) in (2:1:1) 5 M HCl: i-PrOH:THF (100 mL) was stirred 16 h at rt. The mixture was concentrated to remove the THF and i-PrOH. The resulting solution consisting of the product in aqueous HCl was quenched by slow addition to a solution of saturated aqueous NaHCO3 (500 mL) containing excess solid NaHCO3 (28 g). The aqueous layer was extracted with CH2Cl2 (3×100 mL), the organic layers combined and washed with saturated aqueous NaCl (100 mL), dried (MgSO4), and concentrated to give the crude product as a brown oil. The product was purified by ISCO (0-10% EtOAc/Hexanes) to give 1-(3-hydroxy-6-neopentylpyridin-2-yl)ethanone (1.98 g, 64% yield) as a clear, colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163909B2
Source datasetuspto-grants-2012_04
ORD IDord-9c58c76c457249f0996915003a45145f
Source noteuspto-grants-2012_04