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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1084773Generated: October 30, 2026

Sodium Hydroxide → 6-Phenoxy-2-pyridylmethyl 2-ethyl-2-methylbutyl ether

https://huagongshe.com/reaction/1084773

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant2,2-Diethyl-1-propanolHCID 87605—
Reactant2-Chloromethyl-6-phenoxypyridineHCID 13849241—
CatalystTetrabutylammonium BromideHCID 74236—
SolventTolueneHCID 1140—
Product6-Phenoxy-2-pyridylmethyl 2-ethyl-2-methylbutyl etherHCID 1487900071.9%

Reaction Steps

Under a nitrogen atmosphere, 3.83 g of a 45% aqueous sodium hydroxide solution, 120 mg of tetrabutylammonium bromide and 5 ml of toluene were mixed, and to the resulting mixture solution, a solution of 1.0 g of 2-ethyl-2-methylbutanol and 1.51 g of 6-phenoxy-2-chloromethylpyridine in 5 ml of toluene was added at room temperature. After stirring at room temperature for 16 hours, the reaction solution was poured into dilute hydrochloric acid-ice water and extracted twice with toluene. The toluene layers were combined, washed with a saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The residue was subjected to column chromatography on silica gel (developing solvent, n-hexane: ethyl acetate=50:1) to obtain 1.48 g of desired 6-phenoxy-2-pyridylmethyl 2-ethyl-2-methylbutyl ether [present compound (35)] as a colorless oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05006538
Source datasetuspto-grants-1991_04
ORD IDord-1b780f3b456c487b80e83376170b96df
Source noteuspto-grants-1991_04