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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1268491Generated: October 31, 2026

Potassium Carbonate → HCID 22723477, compound

https://huagongshe.com/reaction/1268491

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantDiphenylamineHCID 11487—
ReactantEthanamine, 2-(2-methoxyethoxy)-N,N-bis[2-(2-methoxyethoxy)ethyl]-HCID 112414—
Reactant2-Bromo-9,9-didecyl-7-iodo-9H-fluoreneHCID 22723476—
CatalystCopperHCID 23978—
ProductHCID 22723477HCID 2272347761%

Reaction Steps

A mixture of 2-bromo-7-iodo-9,9-didecylfluorene (52.13 g, 0.08 mol), diphenylamine (15.6 g, 0.0922 mol, 1.152 eq), potassium carbonate (25.5 g, 0.1844 mol), tris(2-(2-methoxyethoxy)ethyl)amine (TDA-1, 5 mL), copper bronze (3.0 g, 0.05 g atom) and xylenes (75 mL) was brought to reflux, and 35 mL, of xylenes were distilled off to reach a reaction temperature of 160° C. The reaction was maintained at this temperature for 18 hours. Some more solvent was distilled off to reach a reaction temperature of 175° C., where the reaction was held for additional 6 hours. The mixture was then cooled, diluted with 100 mL toluene, filtered, the filtrate was concentrated, and the residue was transferred to a column of 600 g of silica gel. Elution with 750 mL hexanes returned a mixture of dibromo and bromoiodo fluorenes as an oil, 10.3 g Elution with heptane-toluene, 1:1, gave the product, 33.48 g (61 % yield, 77% yield on consumed bromoiodo fluorene), m.p. 66.8-69.2° C. Mass Spec: 691, 693 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06555682B1
Source datasetuspto-grants-2003_04
ORD IDord-b66336f344e3485980f163c905cea772
Source noteuspto-grants-2003_04