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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2226112Generated: October 30, 2026

Water → 5-[(2-Methoxyethoxy)methoxy]-2-pyridinecarboxaldehyde

https://huagongshe.com/reaction/2226112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant1-(Chloromethoxy)-2-methoxyethaneHCID 77590—
Reactant5-Hydroxy-2-pyridinecarboxaldehydeHCID 278389—
SolventDimethylformamideHCID 6228—
Product5-[(2-Methoxyethoxy)methoxy]-2-pyridinecarboxaldehydeHCID 19961521—

Reaction Conditions

Temperature25 °C

Reaction Steps

##STR94## A. Methoxyethoxymethyl chloride (MEM) (19 g, 153 mmol) was added to a solution of 5-hydroxy-2-pyridinecarboxaldehyde (18.4 g, 149 mmol)in 300 ml DMF. NaH (6.3 g of 60% oil dispersion, 158 mmol) were added in portions while cooling the mixture to maintain 20°-30° C. The mixture was stirred an additional 1 hour at 25° C. 5 ml water were added, most of the solvent was evaporated, and water was added to the residue. The mixture was extracted with EtOAc. The extracts were dried over Na2SO4, filtered, and evaporated to a residue. The residue was chromatographed on silica gel eluting with EtOAc-hexanes (35:65) to obtain 5-[(2-methoxyethoxy)methoxy]-2-pyridinecarboxaldehyde: C10H13NO4 (211.22); 1H-NMR (CDCl3) δ 10.01 (s,1), 8.52 (d,1), 7.93 (d,1), 7.49 (m,1), 5.39 (s,2), 3.80 (m,2), 3.53 (m,2), 3.32 (s,3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05346898
Source datasetuspto-grants-1994_09
ORD IDord-b1c9c425531f428bbb46db50ef838610
Source noteuspto-grants-1994_09