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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1871049Generated: October 30, 2026

Hexane → HCID 178506829, compound

https://huagongshe.com/reaction/1871049

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
Reactant2,4,7-trimethyl-1H-indeneHCID 11062660—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178506829HCID 178506829—

Reaction Steps

To a solution of 2,4,7-trimethylindene (2.90 g, 18.3 mmol) in 50 ml of THF at 0° C. was added dropwise a 1.6 molar solution of butyllithium in hexane (11.45 ml, 18.3 mmol) in order to produce 2,4,7-trimethylindenyllithium. The solution was stirred for 6 h at room temperature and then added via a cannula to a solution of 1-(9-fluorenyl)-2-bromoethane (5.00 g, 18.3 mmol) in 30 ml THF cooled at -10° C. The mixture was stirred overnight at room temperature and then hydrolyzed with 50 ml of aqueous NH4Cl. The organic phase was separated and the aqueous layer was extracted with ether. The combined organic phases were dried on MgSO4, filtered and the solvent was removed. The residue was crystallized from hot 100% ethanol to give 1.86 g (29%) of 1-(9-fluorenyl)-2-[1-(2,4,7-trimethyl)indenyl]ethane precursor as a white solid; melting point 178-179° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06100416
Source datasetuspto-grants-2000_08
ORD IDord-0577fdd2240a4de4957ee40c222c2f7b
Source noteuspto-grants-2000_08