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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019409Generated: October 26, 2026

Ethyl Acetate → 7-Benzyloxy-6-methoxy-4-(3,4,5-trimethoxyphenyl)isocoumarin-3-carboxylic acid

https://huagongshe.com/reaction/1019409

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
ReactantDI-Tert-butyl bromomalonateHCID 11392273—
ReactantHCID 18398860HCID 18398860—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product7-Benzyloxy-6-methoxy-4-(3,4,5-trimethoxyphenyl)isocoumarin-3-carboxylic acidHCID 1839897371.5%

Reaction Steps

To a solution of 5-benzyloxy-4-methoxy-2-(3,4,5-trimethoxybenzoyl)-benzoic acid (90 g) in dimethylformamide (900 MI) are added potassium carbonate (60.5 g) and di-tert-butyl bromomalonate (64.6 g), and the mixture is stirred at room temperature for three hours. To the reaction mixture are added ethyl acetate and water. The ethyl acetate layer is separated, washed, dried, and concentrated under reduced pressure. To the residue is added a 4M solution of hydrogen chloride in ethyl acetate (500 ml), and the mixture is stirred at room temperature for five hours. The precipitated crystals are collected by filtration, washed, dried, and dissolved in a mixture of acetic acid (40 ml) and dioxane (80 ml). The mixture is heated under reflux for five hours, and the precipitated crystals are collected by filtration. washed, and dried to give 7-benzyloxy-6-methoxy-4-(3,4,5-trimethoxyphenyl)isocoumarin-3-carboxylic acid (70.0 g) as listed in Table 59.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06486155B1
Source datasetuspto-grants-2002_11
ORD IDord-fb36f78292b646ba8b2aa08b4252d083
Source noteuspto-grants-2002_11