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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1940472Generated: October 27, 2026

Indene → Cinnamyl indene

https://huagongshe.com/reaction/1940472

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndeneHCID 7219—
ReactantBenzene, (3-chloro-1-propenyl)-HCID 94242—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductCinnamyl indeneHCID 5436812562%

Reaction Steps

A solution of 98% indene (364 mmoles) in 300 ml of THF was cooled to -78° C. under argon. An equimolar amount of n-butyllithium was added to the solution. The resulting mixture was allowed to warm to room temperature. It was then charged to an equimolar amount of 95% cinnamyl chloride (58.45 g) in 100 ml of THF at -30° C. The mixture was then allowed to warm to room temperature and react for one hour to form cinnamyl indene. The cinnamyl indene was concentrated down to a residue under strong vacuum, and then washed and concentrated twice with 100 ml of hexane. The residue was washed a third time with 100 ml of warm hexane and filtered while hot. The filtrate was again concentrated down to a residue under vacuum. The cinnamyl indene filtrate melted at 55°-69° C. Recovery yield was 62%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05700748
Source datasetuspto-grants-1997_12
ORD IDord-79137be6626d4d1386f1a39e021fc301
Source noteuspto-grants-1997_12