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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1810812Generated: November 3, 2026

Methyl iodide → 2,7-Dibromo-9-methyl-9H-fluorene

https://huagongshe.com/reaction/1810812

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantDichloromethaneHCID 6344—
Reactant2,7-DibromofluoreneHCID 140073—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2,7-Dibromo-9-methyl-9H-fluoreneHCID 1258980670.3%

Reaction Conditions

Temperature-78 °C

Reaction Steps

2,7-dibromofluorene (30 g, 92.59 mmol) was dissolved in anhydrous THF (300 mL) under nitrogen and cooled to −78° C. To solution at −78° C., added n-butyllithium (40.36 mL, 100.9 mmol) over 5 minutes and allowed reaction stir for another 10 minutes. To reaction, then add methyl iodide (6.29 mL, 100.9 mmol) and allowed reaction to stir at −78° C. for 2.0 hours. The reaction was poured into a mixture of dichloromethane and water. The organic layer was collected, and the water layer was further extracted with dichloromethane. Combined all organic layers and removed solvent via vacuo. The crude material was triturated with hexanes and filtered using Buchner funnel to give white solids (22 g, 70%).1H NMR (500 MHz, CDCl3): δ=7.62 (s, 2H), 7.56-7.58 (d, 2H), 7.48-7.50 (dd, 2H), 3.90-3.94 (q, 1H), 1.49-1.51 (d, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362193B2
Source datasetuspto-grants-2013_01
ORD IDord-70154fed68434283b8893ca80c407809
Source noteuspto-grants-2013_01