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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1050692Generated: October 25, 2026

Toluene → HCID 17929730, compound

https://huagongshe.com/reaction/1050692

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantChloroformHCID 6212—
ReactantHexylamineHCID 8102—
Reactant1H,3H-Naphtho(1,8-cd)pyran-1,3-dione, 6-bromo-HCID 66493—
SolventAcetic AcidHCID 176—
ProductHCID 17929730HCID 1792973074.3%

Reaction Steps

A mixture of 4-bromo-1,8-naphthalic anhydride (21.40 g, 77.2 mmol), n-hexylamine (13.1 mL, 100 mmol), toluene (200 mL), and chloroform (200 mL) was heated to boil for 1 hour. Precipitate formed making stirring difficult. The mixture was acidified with acetic acid, and heating was continued at 90° C. with distillation of chloroform. After all precipitate dissolved, the reaction mixture was poured onto crushed ice (300 g) and acidified with concentrated HCl to pH 1. After the ice melted, the solid was filtered off and dried. The crude product was purified by column chromatography (silica gel, hexane/ethyl acetate 2:1) to give 6-bromo-2-hexyl-1H-benzo[de]isoquinoline-1,3(2H)-dione (20.66 g, 74%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382424B2
Source datasetuspto-grants-2016_07
ORD IDord-cb714efa8ddb440cbca5d203951d57bd
Source noteuspto-grants-2016_07