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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 271011Generated: November 1, 2026

Hexane → HCID 131725130, compound

https://huagongshe.com/reaction/271011

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
Reactant3,6-DI-Tert-butylfluoreneHCID 11140437—
ReactantHCID 22327789HCID 22327789—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 131725130HCID 13172513061%

Reaction Steps

To a solution of 1.70 g (6.1 mmol) of 3,6-di-tert-butylfluorene in 40 ml of THF, 3.9 ml (6.4 mmol) of a hexane solution of n-butyllithium was dropwise added in a nitrogen atmosphere with ice cooling, followed by stirring at room temperature for one night. To the resulting red solution, a solution of 1.22 g (6.4 mmol) of 3-(1,1-dimethylbutyl)-6,6-dimethylfulvene in 35 ml of THF was dropwise, added in a nitrogen atmosphere with ice cooling, followed by stirring at room temperature for one night. After the reaction solution was diluted with 100 ml of ether, 50 ml of water was added. The separated organic phase was washed with water and a saturated saline solution, then dried over magnesium sulfate and filtered. From the filtrate, the solvent was removed under reduced pressure to obtain a liquid. The liquid was isolated and purified by column chromatography (silica gel, developing solvent: hexane) to obtain 1.73 g (3.69 mmol) of an oily liquid (yield: 61%). The analyzed values are given below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07449533B2
Source datasetuspto-grants-2008_11
ORD IDord-e7d4860d944d4bc18b1ed947fe572def
Source noteuspto-grants-2008_11