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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 840042Generated: October 25, 2026

Anisole → 4'-Methoxyacetophenone

https://huagongshe.com/reaction/840042

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnisoleHCID 7519—
ReactantAcetic AnhydrideHCID 7918—
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
CatalystScandiumHCID 23952—
SolventDiethyl EtherHCID 3283—
SolventNitromethaneHCID 6375—
Product4'-MethoxyacetophenoneHCID 747697.2%

Reaction Conditions

Temperature21 °C

Reaction Steps

The catalytic effect of the scandium salt of 5-trifluoromethanesulfonyl-1,3-dibutyl-2-sulfonyl-barbituric acid, obtained in Example 25, towards a Friedel-Crafts reaction of acylation was evaluated in the following manner. In 40 ml of anhydrous nitromethane, there is added 887 mg (0.7 moles) of the scandium salt of 5-trifluoromethylsulfonyl-1,3-dibutyl-2-sulfonyl-barbituric acid, and 1.08 g (10 mmoles) of anisole and 2.04 g (20 mmoles) of acetic anhydride. After stirring during 10 min at 21° C., the reaction mixture was diluted with 50 ml of ether and the reaction was inhibited with 100 ml of a saturated solution of sodium bicarbonate NaHCO3. After filtration on Celite, the solution was extracted with three fractions of 50 ml ether, then the collected ether phase was washed with a saturated solution of potassium chloride. After drying the ether phase with magnesium sulfate and evaporation, 1.46 g of p-methoxyacetophenone (95% yield) were recovered with a purity characterized by a proton RMN higher than 99%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06365068B1
Source datasetuspto-grants-2002_04
ORD IDord-c6d545108a58405c8cd8f7255340a5c8
Source noteuspto-grants-2002_04