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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1415867Generated: October 26, 2026

1,2-Dibromoethane → 1H-Indene, 3,3'-(1,2-ethanediyl)bis[4,7-dimethyl-

https://huagongshe.com/reaction/1415867

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DibromoethaneHCID 7839—
Reactant4,7-dimethyl-1H-indeneHCID 81458—
ReactantButyllithiumHCID 178418339—
ReactantHCID 178506817HCID 178506817—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product1H-Indene, 3,3'-(1,2-ethanediyl)bis[4,7-dimethyl-HCID 1085999048%

Reaction Conditions

Temperature0 °C

Reaction Steps

38.2 g (265 mmol) of 4,7-dimethylindene was dissolved in 350 ml of tetrahydrofuran and the solution was cooled to 0° C. Then 165 ml of n-butyllithium (1,6M in hexane, 264 mmol) was added dropwise over 2.5 hours. After warming to room temperature and stirring for 4 hours a purple solution of 4,7-dimethylindenyl-lithium was obtained. This solution was cooled to -70° C. and treated dropwise with 25,3 g of 1,2-dibromoethane (135 mmol) in 15 ml of tetrahydrofuran over 35 min. After warming to room temperature, a pale yellow solution was obtained, and then water was added. The organic phase was collected and dried over Na2SO4. The solvent was removed by vacuum evaporation to provide 20 g of crude product (48% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05910464
Source datasetuspto-grants-1999_06
ORD IDord-db2caea8c2df4289a6c2ef1f817c4457
Source noteuspto-grants-1999_06