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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 600164Generated: October 26, 2026

Dimethylformamide → 1-Bromo-3,6,8-tri(4-methylnaphthalene-1-yl)pyrene

https://huagongshe.com/reaction/600164

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantN-bromobutanimideHCID 67184—
Reactant1,3,6-Tri(4-methylnaphthalene-1-yl)pyreneHCID 86628594—
SolventWaterHCID 962—
Product1-Bromo-3,6,8-tri(4-methylnaphthalene-1-yl)pyreneHCID 8662859370.1%

Reaction Steps

A mixed solution of 1.9 g of the above-mentioned 1,3,6-tri(4-methylnaphthalene-1-yl)pyrene, 0.64 g of N-bromosuccinimide and 15 ml of dimethylformamide was stirred under nitrogen gas stream at a temperature of 60° C. for 6 hours. After cooling the mixed solution to room temperature, 50 ml of water was injected thereinto to extract therefrom with 100 ml of dichloromethane. The organic layer was washed twice with 50 ml of water, dried by magnesium sulfate and thereafter concentrated by evaporation. The organic layer was purified by silica gel column chromatography and thereafter vacuum dried under a temperature of 70° C. to obtain 1.5 g of 1-bromo-3,6,8-tri(4-methylnaphthalene-1-yl)pyrene as pale-yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07901794B2
Source datasetuspto-grants-2011_03
ORD IDord-ad961cfacc5549c48c88364599b9bdce
Source noteuspto-grants-2011_03