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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 279004Generated: October 30, 2026

Potassium Iodide → HCID 22623970, compound

https://huagongshe.com/reaction/279004

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromopropionic acidHCID 11729—
ReactantHCID 22624014HCID 22624014—
SolventAcetoneHCID 180—
ProductHCID 22623970HCID 2262397080.3%

Reaction Steps

2-Benzyloxy-5-hydroxy-benzo[de]isoquinoline-1,3-dione (1.1 g, 3.5 mmol) and 2-bromopropionic acid (1.2 g, 7.8 mmol) were reacted in acetone (300 mL) in presence of potassium carbonate (2.3 g, 5.1 mmol) and potassium iodide (0.1 g, 0.6 mmol), following the procedure of Example 22 to give 1.1 g of 2-benzyloxy-5-(2-carboxy-ethoxy)-benzo[de]isoquinoline-1,3-dione. The hydrogenation of 2-benzyloxy-5-(2-carboxy-ethoxy)-benzo[de]isoquinoline-1,3-dione (1.1 g) in the presence of 10% Pd/C (0.5 g) in DMA (20 mL) afforded 0.3 g of the title compound, mp 236-239° C.;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06362181B1
Source datasetuspto-grants-2002_03
ORD IDord-0228dba098d34a51859df3cd7a70e588
Source noteuspto-grants-2002_03