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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2305715Generated: October 25, 2026

Sodium Chloride → 5-(3-Chloropropoxy)-3-(phenylmethoxy)pyridine

https://huagongshe.com/reaction/2305715

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantSodium hydrideHCID 24758—
Reactant1-Chloro-3-iodopropaneHCID 81363—
Reactant3-Benzyloxy-5-hydroxypyridineHCID 22989704—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product5-(3-Chloropropoxy)-3-(phenylmethoxy)pyridineHCID 22989698—

Reaction Steps

Under a nitrogen atmosphere, a solution of 5-(phenylmethoxy)-pyridine-3-ol (1.52 g, 7.56 mmol) in N,N-dimethylformamide (DMF) (10 mL) was added drop-wise over 5 min to a cold (0-5° C.), stirring slurry of sodium hydride (0.238 g of an 80% dispersion in mineral oil, 7.94 mmol) in DMF (15 mL). The mixture was allowed to stir and warm to ambient temperature over 1 h. Next, 1-chloro-3-iodopropane (1.85 g, 9.07 mmol) was added drop-wise over 5 min. The resulting dark-brown mixture was stirred at ambient temperature for 4 h. Water (25 mL) was added, followed by saturated NaCl solution (25 mL), and the mixture was extracted with ether (4×50 mL). The combined ether extracts were dried (Na2SO4), filtered, and concentrated by rotary evaporation to a residue that was dried briefly under high vacuum to give an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06441006B2
Source datasetuspto-grants-2002_08
ORD IDord-2f24f7d47e284563a8fe202d5507abd5
Source noteuspto-grants-2002_08