Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2180357Generated: October 30, 2026

1-Chloro-2-nitrobenzene → HCID 618469, compound

https://huagongshe.com/reaction/2180357

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-2-nitrobenzeneHCID 6945—
Reactant2-MethoxyanilineHCID 7000—
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantSodium t-butoxideHCID 23676156—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventDiethyl EtherHCID 3283—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventDodecaneHCID 8182—
ProductHCID 618469HCID 61846982%

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of ligand 1 (see FIG. 1) [42 mg, 0.1 mmol (8.4 mg, 0.02 mmol, 4 mol % per reaction)] and NaOt-Bu [10 mg, 0.1 mmol (2 mg, 0.02 mmol, 4 mol % per reaction)] were stirred in 5 mL DME (anhy). After 10 minutes, 1 mL of the solution was added via syringe to a test tube containing (under an Argon atmosphere) Pd2(dba)3 (4.6 mg, 0.005 mmol, 2 mol % Pd), K3PO4 (148 mg, 0.7 mmol), 2-chloronitrobenzene (79 mg, 0.5 mmol), and o-anisidine (68 μL, 0.6 mmol). The test tube was capped (with a proper cap-no rubber septa) and heated at 100° C. for 18 hours. The reaction mixture was allowed to cool to r.t., diluted with ether and dodecane was added as an internal standard (the consumption of the aryl chloride was incomplete). The reaction mixture was purified by column chromatography (5% EtOAc/hexanes) to yield 100 mg (82% yield) of the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06888029B2
Source datasetuspto-grants-2005_05
ORD IDord-af42405ea6444967a664fef8250bd764
Source noteuspto-grants-2005_05