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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1404882Generated: October 31, 2026

Methanol → 1-Bromo-7-(tert-butyl)pyrene

https://huagongshe.com/reaction/1404882

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
Reactant2-Tert-butylpyreneHCID 11817768—
ReactantBenzyltrimethylammoniumtribromideHCID 53442637—
SolventDichloromethaneHCID 6344—
Product1-Bromo-7-(tert-butyl)pyreneHCID 49765730142.7%

Reaction Steps

Then, a mixed solution of 3 g (content 65%) of 2-t-butylpyrene, 50 ml of dichloromethane and 15 ml of methanol was cooled to 0° C. under a nitrogen stream, and 3.3 g of benzyltrimethylammonium tribromide dissolved in 10 ml of dichloromethane was added dropwise. After this mixed solution was stirred at room temperature for 2 hours, 50 ml of water was added, and this was extracted with 50 ml of dichloromethane. The organic layer was washed with 50 ml of water two times, dried with magnesium sulfate, and evaporated. To the resulting solid was added 10 ml of methanol, and the mixture was stirred for 10 minutes, and filtered. Further, 30 ml of hexane was added, and the mixture was stirred for 30 minutes, and filtered. After the resultant was vacuum dried, 2.3 g of 1-bromo-7-t-butylpyrene was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916275B2
Source datasetuspto-grants-2014_12
ORD IDord-e21ea0c3b14341de82793ac4674136f7
Source noteuspto-grants-2014_12