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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1009681Generated: October 31, 2026

Hexane → HCID 178478636, compound

https://huagongshe.com/reaction/1009681

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantHCID 5474041HCID 5474041—
Reactant2-(1H-inden-3-ylmethyl)pyridineHCID 12124590—
ReactantTetrahydrofuran;trichlorochromiumHCID 25155609—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178478636HCID 178478636—

Reaction Conditions

Temperature-100 °C

Reaction Steps

A solution of 52.7 g of the above mixture of 2-(1H-inden-3-ylmethyl)pyridine and 2-[(E)-2,3-dihydro-1H-inden-1-ylidenemethyl]pyridine in a molar ratio of 10:9 in 550 ml of tetrahydrofuran was cooled to −100° C. 80.5 ml of a 15% strength n-butyllithium solution in hexane (0.1288 mol) were then slowly added dropwise. After the addition was complete, the reaction mixture was stirred at −100° C. for a further 45 minutes. The mixture was subsequently allowed to warm to room temperature. After stirring for a further 2 hours, the solution was cooled to 60° C. and 49 g (0.1288 mol) of chromium trichloride tris(tetrahydrofuran) were added while stirring. The mixture was allowed to warm slowly to room temperature and was subsequently stirred for a further 10 hours at room temperature. The reaction mixture was then refluxed for 20 minutes and subsequently cooled to room temperature. The solid which had precipitated was filtered off and washed with hot tetrahydrofuran. The solid was subsequently washed with diethyl ether and dried under reduced pressure. This gave 24.9 g of (1-(2-pyridylmethyl)indenyl)chromium dichloride (59%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973114B2
Source datasetuspto-grants-2011_07
ORD IDord-ac90dc4b4ee94fa2adb1b4288b83bc59
Source noteuspto-grants-2011_07