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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2273531Generated: October 30, 2026

Sodium → 5-(Benzyloxy)-2-(methoxymethyl)pyridine

https://huagongshe.com/reaction/2273531

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodiumHCID 5360545—
ReactantSodium MethoxideHCID 10942334—
Reactant5-(Benzyloxy)-2-(chloromethyl)pyridineHCID 17854158—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
Product5-(Benzyloxy)-2-(methoxymethyl)pyridineHCID 5750035094%

Reaction Steps

50 g (0.21 mol) of 5-benzyloxy-2-chloromethylpyridine (CAS 127590-90-3; D. I. Scopes, N. F. Norman, D. E. Bays, D. Belton, J. Brain et al., J. Med. Chem., 1992, 35, 490-501) in solution in 150 ml of methanol are added to the solution of sodium methoxide prepared by adding 6.4 g (0.28 mol) of sodium to 150 ml of methanol. After refluxing for 3 hours under nitrogen, the solution is concentrated to dryness. The oil obtained is taken up in ethyl acetate. The solution is washed with a saturated aqueous solution of sodium chloride, dried over anhydrous sodium sulphate and then concentrated to dryness. 46 g (94%) of a brown oil are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120819B2
Source datasetuspto-grants-2015_09
ORD IDord-b8b85eca74ed441eb2fe664f4b940ceb
Source noteuspto-grants-2015_09