Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 278996Generated: October 27, 2026

Methanol → 2-Benzyloxy-6-methoxy-benzo[de]-isoquinoline-1,3-dione

https://huagongshe.com/reaction/278996

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium hydrideHCID 24758—
Reactant2-Benzyloxy-6-bromo-benzo[de]isoquinoline-1,3-dioneHCID 22624038—
Product2-Benzyloxy-6-methoxy-benzo[de]-isoquinoline-1,3-dioneHCID 22623910—

Reaction Steps

2-Benzyloxy-6-bromo-benzo[de]isoquinoline-1,3-dione (3.2 g, 8.4 mmol, from Example M) was added to a solution of sodium hydride (0.5 g, 12.5 mmol) in methanol (100 mL). The mixture was refluxed for 8 hours and concentrated in vacuo. The solid residue was dissolved in water and acidified with concentrated HCl to pH 4. The resulting precipitate was filtered, washed with water, and dried to give 0.8 g of 2-benzyloxy-6-methoxy-benzo[de]-isoquinoline-1,3-dione. The hydrogenation of 2-benzyloxy-6-methoxy-benzo[de]isoquinoline-1,3-dione (0.6 g) in the presence of Pd/C (10%) in DMA (20 mL) afforded 0.2 g of the title compound, mp 267-269° C.;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06362181B1
Source datasetuspto-grants-2002_03
ORD IDord-c3a75562c94348838a2a35723cd33c83
Source noteuspto-grants-2002_03