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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 883001Generated: November 3, 2026

3-Bromoanisole → N-Cyclopropyl-3-methoxyaniline

https://huagongshe.com/reaction/883001

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromoanisoleHCID 16971—
ReactantCyclopropylamineHCID 69828—
ReactantBinap, (A+-)-HCID 634876—
ReactantSodium t-butoxideHCID 23676156—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
ProductN-Cyclopropyl-3-methoxyanilineHCID 45091015—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a high-pressure tube was added 3-bromoanisole (0.250 mL, 2 mmol), cyclopropylamine (0.225 mL, 3.2 mmol), sodium t-butoxide (0.29 g, 3.0 mmol), (+/−) BINAP (0.04 g, 0.06 mmol), and Pd2(dba)3 (0.010 g, 0.01 mmol). This mixture was suspended in 4 mL anhydrous toluene. The tube was flushed with dry nitrogen gas, then capped and wrapped in aluminum foil. The reaction mixture was stirred and heated to 80° C. overnight, then allowed to cool, and the reaction vessel was opened. The mixture was diluted with diethyl ether, filtered through Celite, and the filtrate was concentrated to a yellow oil. LC/MS analysis showed one peak with the correct mass, and due to the limited stability of the material, it was carried through without further purification. FIA MS 164 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08236815B2
Source datasetuspto-grants-2012_08
ORD IDord-e2fe15a64210493a9846e6fa9c7f77fe
Source noteuspto-grants-2012_08