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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388242Generated: October 26, 2026

Toluene → 2-Cyclopropyl 5-nitrobenzenamine

https://huagongshe.com/reaction/388242

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantCesium carbonateHCID 10796—
Reactant2-Bromo-5-nitroanilineHCID 82607—
Reactant2-Cyclopropyl-6-methyl-1,3,6,2-dioxazaborocane-4,8-dioneHCID 44138342—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
Product2-Cyclopropyl 5-nitrobenzenamineHCID 5806580170%

Reaction Steps

In a 250 mL round bottom flask to a solution of 2-bromo 5-nitroaniline (2.30 g, 10.60 mmol) in toluene (90 mL) tricyclohexylphosphine (0.89 g, 3.18 mmol), Cs2CO3 (17.22 g, 52.99 mmol), cyclopropylboronic acid MIDA ester (2.92 g, 14.84 mmol) and 10 ml de-ionized water were added and the solution was degassed with nitrogen for 30 minutes. To the above solution Pd(OAc)2 (0.36 g, 1.59 mmol) was added under nitrogen and the reaction mixture was refluxed for 12 hours. LC MS analysis of the crude reaction indicated the completion of the reaction. The crude reaction mixture was filtered on celite pad and the volatiles were removed under reduced pressure. The dark brown oil was worked-up with 2×100 mL ethyl acetate and water (100 mL), dried on MgSO4 and ethyl acetate was evaporated under reduced pressure. The crude reaction mixture was separated by column chromatography to give Compound 13 in 70% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08377924B2
Source datasetuspto-grants-2013_02
ORD IDord-28594c669c8c4fb8ad2cc5894f257626
Source noteuspto-grants-2013_02