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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2352405Generated: October 27, 2026

Diethyl Ether → 5-(3,3-Dimethylbutanoyl)-3-methyl-1,2-di(2-[2-(2-tetrahydropyranyloxy)ethoxy]ethoxy)benzene

https://huagongshe.com/reaction/2352405

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantPotassium CarbonateHCID 11430—
Reactant2-[2-(2-Chloroethoxy)ethoxy]oxaneHCID 10965737—
Reactant3-Methyl-5-(3,3-dimethylbutanoyl)catecholHCID 14279312—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product5-(3,3-Dimethylbutanoyl)-3-methyl-1,2-di(2-[2-(2-tetrahydropyranyloxy)ethoxy]ethoxy)benzeneHCID 14675607—

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 3-methyl-5-(3,3-dimethylbutanoyl)catechol (12 g, 0.054 mole), 2-(2-[2-chloroethoxy]ethoxy)tetrahydropyran (24.8 g, 0.119 mole) and potassium carbonate (16.6 g, 0.12 mole) in 100 ml dimethyformamide was stirred under a nitrogen atmosphere at 140° C. for 16 hours. The reaction mixture was cooled to 25° C. and 500 ml diethyl ether and 300 ml water were added. The layers were separated and the organic layer was washed with four 250 ml portions of water and 100 ml brine, dried over anhydrous magnesium sulfate and the solvent evaporated in vacuo. The resulting brown oil was purified by column chromatography over silica gel with 10% ethyl acetate--90% chloroform. The title compound was isolated as a yellow oil (13.5 g, 44% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04876367
Source datasetuspto-grants-1989_10
ORD IDord-3ef3cb22500c4566a4c9f787a99539b7
Source noteuspto-grants-1989_10