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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | 4,7-dimethyl-1H-indene | HCID 81458 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Reactant | HCID 178506817 | HCID 178506817 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1H-Indene, 3,3'-(1,2-ethanediyl)bis[4,7-dimethyl- | HCID 10859990 | 48% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05910464 |
|---|
| Source dataset | uspto-grants-1999_06 |
|---|
| ORD ID | ord-db2caea8c2df4289a6c2ef1f817c4457 |
|---|
| Source note | uspto-grants-1999_06 |
|---|