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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2040745Generated: October 31, 2026

Dichloromethane → 7-Fluoro-3,4,4a,5-tetrahydro-2H-indeno[1,2-b]pyridine

https://huagongshe.com/reaction/2040745

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriethylamineHCID 8471—
Reactant3-BromopropylamineHCID 78702—
Reactant5-Fluoro-1-indanoneHCID 136537—
CatalystDiamminetetrachlorotitanate(IV)HCID 160960—
SolventDimethylformamideHCID 6228—
Product7-Fluoro-3,4,4a,5-tetrahydro-2H-indeno[1,2-b]pyridineHCID 14075057—

Reaction Conditions

Temperature0 °C

Reaction Steps

3-Bromopropylamine (4.7 g. 21.7 mmole) and 5-Fluoro-1-indanone (2.5 g, 16.7 mmole) were dissolved in 50 ml DMF and the reaction was cooled to 0° C. Triethylamine (13.5 g, 133 mmole) was added. 20 ml DCM was also added to help with the stirring. Titanium chloride (1M in DCM, 15 ml) was then added and the ice bath was removed. The reaction was stirred at room temperature overnight. 200 ml ether was added and the reaction was filtered though a Celite cake. The filtrate was concentrated to dryness under vacuum. The residue was dissolved in 200 ml ether and washed with brine (2×200 ml). The organic layer was dried over sodium sulfate and concentrated to dryness. 2.6 g Black oil was obtained and it was used in next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580956B2
Source datasetuspto-grants-2013_11
ORD IDord-36384d1985414c868f5e2a91fc2bb6bb
Source noteuspto-grants-2013_11