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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 873497Generated: October 29, 2026

Potassium Iodide → 2,7-Dibromo-9,9-dibutyl-9H-fluorene

https://huagongshe.com/reaction/873497

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantButyl bromideHCID 8002—
ReactantPotassium HydroxideHCID 14797—
Reactant2,7-DibromofluoreneHCID 140073—
Catalyst18-Crown-6HCID 28557—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2,7-Dibromo-9,9-dibutyl-9H-fluoreneHCID 22475893159.8%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 12.0 g (37 mmol) of 2,7-dibromofluorene 2-7, 12 mL (111 mmol) of 1-bromobutane, 6.3 g (1 mmol) of potassium hydroxide, 0.9 g (6 mmol) of potassium iodide, 0.29 g (1 mmol) of 18-crown-6 and 120 mL of DMF was stirred and heated to 90° C. for overnight under N2. After cooling to room temperature, the solution was poured to cold water and extracted with dichloromethane (3×50 mL). The combined organic layer was washed with water, dried over anhydrous NaSO4, filtered and evaporated to dryness. The crude product was purified by silica gel column chromatography using petroleum ether as eluent affording the desired product as a white solid (12.9 g, 80%). Mp: 116.8-118.5° C. 1H NMR (400 MHz, CDCl3, δ) 7.53 (d, J=8.8 Hz, 2H), 7.46 (dd, J=7.2 Hz, J=2.2 Hz, 4H), 1.90-1.94 (m, 4H), 1.06-1.11 (m, 4H), 0.70 (t, J=7.4 Hz, 3H), 0.54-0.59 (m, 4H). 13C NMR (100 MHz, CDCl3, δ) 152.5, 139.1, 130.2, 126.2, 121.5, 121.2, 55.6, 40.1, 25.8, 22.9, 13.8. MS (FAB) m/z 436.1 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975419B2
Source datasetuspto-grants-2015_03
ORD IDord-9bd15d22e07f4cc18b9a4b1ebd09d28b
Source noteuspto-grants-2015_03