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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643276Generated: October 27, 2026

9-Methyl-3,9-diazabicyclo[3.3.1]nonane → 3-(3,4-Dichloro-phenyl)-9-methyl-3,9-diaza-bicyclo[3.3.1]nonane Fumaric Acid Salt

https://huagongshe.com/reaction/643276

Reaction equation

Participants

RoleNameHCIDCharge
Reactant9-Methyl-3,9-diazabicyclo[3.3.1]nonaneHCID 18911—
Reactant4-Bromo-1,2-dichlorobenzeneHCID 29013—
ReactantFumaric AcidHCID 444972—
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
ReactantPotassium tert-butoxideHCID 23665647—
Catalystpalladium(II) acetateHCID 167845—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Solvent1,4-DioxaneHCID 31275—
Product3-(3,4-Dichloro-phenyl)-9-methyl-3,9-diaza-bicyclo[3.3.1]nonane Fumaric Acid SaltHCID 131728060—

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 9-methyl-3,9-diaza-bicyclo[3.3.1]nonane (0.50 g, 3.56 mmol), 1-bromo-3,4-dichlorobenzene (1.61 g, 7.13 mmol), potassium tert-butoxide (0.80 g, 7.13 mmol), 2-dicyclohexylphosphino-2′,4′,6′-triisopropyl-1,1′-biphenyl (0.050 g, 0.105 mmol) and palladium (II) acetate (0.025 g, 0.111 mmol) and dioxane (10 ml) was stirred at 110° C. for 20 min. Water (30 ml) was added followed by extraction with ethylactate (3×10 ml). The organic phase was dried and evaporated. The crude product was purified by silica gel column chromatography using a solvent mixture of dichloromethane, methanol and aqueous ammonia (18-1-1%). The pure product was isolated. Yield 211 mg (20%). The fumarate salt was precipitated from 1.1 eq of fumaric acid and a mixture of ethanol and diethylether (2:5). Mp 187-189° C. LC-ESI-HRMS of [M+H]+shows 285.092 Da. Calc. 285.092529 Da, dev. −1.9 ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700596B2
Source datasetuspto-grants-2010_04
ORD IDord-33066f9569544f388e49dc56084b56d8
Source noteuspto-grants-2010_04