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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2236644Generated: October 31, 2026

Acetic Anhydride → 4-methoxymethylene-6-bromo-4H-isoquinoline-1,3-dione

https://huagongshe.com/reaction/2236644

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTrimethyl orthoformateHCID 9005—
Reactant6-Bromoisoquinoline-1,3-diolHCID 12023317—
SolventDimethylformamideHCID 6228—
Product4-methoxymethylene-6-bromo-4H-isoquinoline-1,3-dioneHCID 68692764—

Reaction Conditions

Temperature125 °C

Reaction Steps

To a suspension of 6-Bromo-4H-isoquinoline-1,3-dione (120 mg, 0.5 mmol) in 1.25 mL of a 4:1 mixture of acetic anhydride and N,N-dimethylformamide, respectively, is added trimethylorthoformate (110 μL, 1.0 mmol). The reaction mixture is shaken in a heating block at 125° C. for 1 hour. Upon cooling to room temperature, the product precipitated out. The precipitate is then filtered off, rinsed with copious amounts of ether, and dried to yield 126.3 mg of 6-bromo-4-methoxymethylene-4H-isoquinoline-1,3-dione.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07713994B2
Source datasetuspto-grants-2010_05
ORD IDord-0c6db442cc884550b0f3c66fce5c694c
Source noteuspto-grants-2010_05