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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1484772Generated: October 25, 2026

Chloromethyl Methyl Ether → 2-(Benzyloxy)-5-(methoxymethoxy)pyridine

https://huagongshe.com/reaction/1484772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloromethyl Methyl EtherHCID 7864—
ReactantSodium hydrideHCID 24758—
Reactant6-(Benzyloxy)pyridin-3-olHCID 42553041—
SolventDimethylformamideHCID 6228—
Product2-(Benzyloxy)-5-(methoxymethoxy)pyridineHCID 6721768487%

Reaction Conditions

Temperature2.5 °C

Reaction Steps

To a solution of 6-(benzyloxy)pyridin-3-ol (2.0 g, 10 mmol, 1 eq.) in DMF (20 mL) was added NaH (60% in mineral oil; 0.6 g, 15 mmol, 1.5 eq.) at 0-5° C. portion-wise. Upon the completion of addition, the mixture was continued to stir at 0-5° C. for 15 min, added chloromethyl methyl ether (0.88 g, 11 mmol, 1.1 eq.), stirred at 0-5° C. for another 20 min, and quenched with NH4Cl(sat) solution. The aqueous layer was extracted with EtOAc (3×20 mL) and the combined organic layers were washed with water and brine, dried over Na2SO4, concentrated, and purified on silica gel using 25% EtOAc/hexanes as eluent to give 2-(benzyloxy)-5-(methoxymethoxy)pyridine (2.1 g, 87%) as a colorless oil. MS (ESI) m/z 246.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422279B2
Source datasetuspto-grants-2016_08
ORD IDord-b67882bc98c9423cb220948f069a348e
Source noteuspto-grants-2016_08