Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844033Generated: November 1, 2026

O-Xylene → 4-Cyclopropyl-3-nitropyridine

https://huagongshe.com/reaction/1844033

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-XyleneHCID 7237—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Chloro-3-nitropyridineHCID 2735781—
ReactantCyclopropylboronic acidHCID 2760897—
CatalystHCID 178418397HCID 178418397—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
Product4-Cyclopropyl-3-nitropyridineHCID 66801854736.3%

Reaction Conditions

Temperature130 °C

Reaction Steps

4-Chloro-3-nitropyridine (100 mg, 0.630 mmol) and cyclopropyl boronic acid (10.0 mg, 0.091 mmol) were added to a solution of xylene (3 mL) previously purged with argon (10 min). The reaction mixture was purged with argon for a further 15 mins, followed by the addition of potassium carbonate (174.35 mg, 1.26 mmol) and Pd(PPh3)4 (34.5 mg, 0.063 mmol). The resulting mixture was heated to reflux at 130° C. overnight. The reaction was monitored by TLC (30% ethyl acetate in hexane). The reaction mixture was cooled and concentrated to afford the crude product. Purification by column chromatography on silica gel (15% ethyl acetate in hexane) afforded 110 mg of the product (100% yield). LCMS: 99.09%, m/z=165 (M+1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946260B2
Source datasetuspto-grants-2015_02
ORD IDord-30041b14b6114ed2b7384ac79b9e3e78
Source noteuspto-grants-2015_02