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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030684Generated: October 26, 2026

Tetrahydrofuran → 2'-Hydroxy-4',6'-bis(methoxymethoxy)-3'-(2-propenyl)acetophenone

https://huagongshe.com/reaction/1030684

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantDimethyl EtherHCID 8254—
ReactantDiisopropylethylamineHCID 81531—
Reactant2',4',6'-Trihydroxy3'-(2-propenyl)acetophenoneHCID 14368078—
Product2'-Hydroxy-4',6'-bis(methoxymethoxy)-3'-(2-propenyl)acetophenoneHCID 1974488594.7%

Reaction Steps

In 160 ml of anhydrous tetrahydrofuran were dissolved 18.4 g of the so-obtained 2',4',6'-trihydroxy3'-(2-propenyl)acetophenone and 57.1 g of N,N-diisopropylethylamine, and 28.4 g of chrolomethyl methyl ether was added to the solution under ice cooling and the reaction mixture was stirred under ice cooling for 1 hour, and further, stirred at room temperature for 4 hours to effect a reaction. The reaction mixture was extracted with diethyl ether and filtered, and the solvent was removed from the filtrate by distillation. The obtained residue was subjected to the silica gel column chromatography [eluting solvent=n-hexane/ethyl acetate (7/1)] to obtain 24.8 g (yield=94.7%) of 2'-hydroxy-4',6'-bismethoxymethoxy-3'-(2-propenyl)acetophenone in the form of a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05106871
Source datasetuspto-grants-1992_04
ORD IDord-7a22d84775e5409a8259bce92fa8e549
Source noteuspto-grants-1992_04