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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1043673Generated: October 31, 2026

Diethyl Ether → 8-Methoxymethoxy-2,2,4-trimethyl-1,2-dihydro-6-oxa-1-azachrysen-5-one

https://huagongshe.com/reaction/1043673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant8-Hydroxy-2,2,4-trimethyl-1,2-dihydro-6-oxa-1-azachrysen-5-oneHCID 57990611—
SolventDimethylformamideHCID 6228—
Product8-Methoxymethoxy-2,2,4-trimethyl-1,2-dihydro-6-oxa-1-azachrysen-5-oneHCID 5799060366%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 8-hydroxy-2,2,4-trimethyl-1,2-dihydro-6-oxa-1-azachrysen-5-one (Reference Compound No. 1-(4), 1.00 g, 3.25 mmol), chlorodimethylether (420 μL, 5.53 mmol) and potassium carbonate (1.35 g, 9.77 mmol) was suspended in anhydrous N,N-dimethylformamide (15 mL) and the suspension was stirred at 50° C. overnight. After cooling down, ethyl acetate (100 mL) and diethylether (100 mL) were added thereto. The whole was washed with water (150 mL, 100 mL) and saturated brine (100 mL) successively, dried over anhydrous magnesium sulfate, and then the solvent was removed under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give the titled reference compound (747 mg) as a yellow solid. (Yield 66%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563551B2
Source datasetuspto-grants-2013_10
ORD IDord-f4c9a8ecc7c944298409d2cfe1f2abf0
Source noteuspto-grants-2013_10