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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2371470Generated: October 30, 2026

2,2-Dimethylbutanol → 6-Phenoxy-2-pyridylmethyl 2,2-dimethylbutyl ether

https://huagongshe.com/reaction/2371470

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2-DimethylbutanolHCID 14454—
ReactantSodium HydroxideHCID 14798—
Reactant2-Chloromethyl-6-phenoxypyridineHCID 13849241—
CatalystTetrabutylammonium BromideHCID 74236—
SolventTolueneHCID 1140—
Product6-Phenoxy-2-pyridylmethyl 2,2-dimethylbutyl etherHCID 1487896823%

Reaction Steps

4.4 Grams of a 45% aqueous sodium hydroxide solution, 100 mg of tetrabutylammonium bromide and 5 ml of toluene were mixed, and to the resulting mixture, a solution of 0.7 g of 2,2-dimethylbutanol and 1.72 g of 2-chloromethyl-6-phenoxypyridine in 10 ml of toluene was added at room temperature under a nitrogen atmosphere. After 12 hours, the reaction solution was poured into hydrochloric acid-ice water and extracted twice with diethyl ether. The ether layers were combined, washed with a saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure, and the residue was treated by preparative thin layer chromatography (developing solvent, hexane:ethyl acetate=5:1) to obtain 0.45 g of desired 6-phenoxy-2-pyridylmethyl 2,2-dimethylbutyl ether [present compound (17)] as an oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05093373
Source datasetuspto-grants-1992_03
ORD IDord-d138186232704f38b3b30e69e9b9f1ef
Source noteuspto-grants-1992_03