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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1471726Generated: October 31, 2026

Potassium Carbonate → 2-(2-Methoxyethoxy)-5-(methoxymethoxy)pyridine

https://huagongshe.com/reaction/1471726

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromoethyl methyl etherHCID 80972—
ReactantHCID 178498305HCID 178498305—
SolventDimethylformamideHCID 6228—
Product2-(2-Methoxyethoxy)-5-(methoxymethoxy)pyridineHCID 8669076727%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a mixture of 5-(methoxymethoxy)pyridin-2-ol (1.35 g, 8.71 mmol, 1 eq.) and K2CO3 (6.01 g, 43.6 mmol, 5.0 eq.) in DMF (30.0 mL) was added 1-bromo-2-methoxyethane (3.61 g, 26.1 mmol, 3 eq.). The mixture was heated at 60° C. for 2 h, cooled, filtered, concentrated, and purified on silica gel using a mixture of EtOAc and hexanes as eluent to give 2-(2-methoxyethoxy)-5-(methoxymethoxy)pyridine (500 mg, 27%) as a colorless oil. 1H NMR (400 MHz, CDCl3) δ 7.94 (d, J=3.0 Hz, 1H), 7.35 (ddd, 18.9, 3.0, 1.0 Hz, 1H), 6.76 (dd, J=8.9, 1.0 Hz, 1H), 5.11 (s, 2H), 4.48-4.40 (m, 2H), 3.79-3.71 (m, 2H), 3.50 (s, 3H), 3.45 (s, 3H). LRMS (M+H+) m/z 214.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012450B2
Source datasetuspto-grants-2015_04
ORD IDord-05d4f7d3d4994b48b8df01d274f51585
Source noteuspto-grants-2015_04