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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 381237Generated: October 27, 2026

Iodoethane → HCID 15913958, compound

https://huagongshe.com/reaction/381237

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantHexaneHCID 8058—
ReactantHCID 11139790HCID 11139790—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15913958HCID 15913958—

Reaction Conditions

Temperature-10 °C

Reaction Steps

1.36 g, 5.26 mmol of 1,2-bis(2-indenyl)ethane, prepared as described in the above reported Synthesis 1(a), were dissolved in 25 mL THF and cooled to −10° C. 5.5 ml of a 1.6 M solution of BuLi in hexane (8.8 mmoles) were added and the resulting orange/brown solution was stirred for 2 hours, at room temperature. To the obtained ;mixture was added, by means of a cannula, a solution of 1.1 ml of EtI (7.1 mmol) in 10 ml THF, at −10° C. After 2 hours, the THF was removed under vacuum, and Et2O was added. The thus obtained ether solution was washed 3 times with a saturated solution of NaHCO3 and 3 times with a saturated aqueous solution of NaCl. After drying over MgSO4, 1.46 g of 1,2-bis(1-ethyl-2-indenyl)ethane was isolated, in the form of a yellow oil. 1H NMR and GC showed that it consisted of the three possible double bond isomers.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06306791B2
Source datasetuspto-grants-2001_10
ORD IDord-8808ef5f89cd400bbcc9d29548c36377
Source noteuspto-grants-2001_10