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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1746154Generated: October 26, 2026

Toluene → 1-Cyclopropyl 3,5-dinitrobenzene

https://huagongshe.com/reaction/1746154

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantCesium carbonateHCID 10796—
Reactant1-Bromo-3,5-dinitrobenzeneHCID 44534—
Reactant2-Cyclopropyl-6-methyl-1,3,6,2-dioxazaborocane-4,8-dioneHCID 44138342—
SolventWaterHCID 962—
Product1-Cyclopropyl 3,5-dinitrobenzeneHCID 5374278764%

Reaction Steps

In a 250 mL round bottom flask to a solution of 3-bromo 1,5-dinitrobenzene (2.1 g, 8.50 mmol) in toluene (90 mL) tricyclohexylphosphine (0.72 g, 2.55 mmol), Cs2CO3 (16.58 g, 51 mmol), cyclopropylboronic acid MIDA ester (2.35 g, 11.90 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 (0.29 g, 1.28 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 8 in 64% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09149475B2
Source datasetuspto-grants-2015_10
ORD IDord-53734062b28f47dab072299d46d4d596
Source noteuspto-grants-2015_10