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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2180360Generated: November 1, 2026

1-Chloro-2-nitrobenzene → HCID 23250451, compound

https://huagongshe.com/reaction/2180360

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-2-nitrobenzeneHCID 6945—
ReactantHexylamineHCID 8102—
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantSodium t-butoxideHCID 23676156—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventDiethyl EtherHCID 3283—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventDodecaneHCID 8182—
ProductHCID 23250451HCID 232504512.7%

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of Pd2(dba)3 [92 mg, 0.1 mmol (4.6 mg, 0.005 mmol, 2 mol % Pd per reaction)], ligand 1 (see FIG. 1) [168 mg, 0.4 mmol (8.4 mg, 0.02 mmol, 4 mol % per reaction)] and NaOt-Bu [40 mg, 0.4 mmol (2 mg, 0.02 mmol, 4 mol % per reaction)] were stirred in 10 mL DME (anhy). After 10 minutes, 0.5 mL of the solution was added via syringe to a test tube containing (under an Argon atmosphere) K3PO4 (148 mg, 0.7 mmol), 2-chloronitrobenzene (79 mg, 0.5 mmol), and hexylamine (79 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 reaction mixture was purified by preparatory TLC (EtOAc/hexanes as the eluent) to yield 3 mg of the desired product (which was used for calibration with the internal standard). The GC yield was calculated to be 19%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06888029B2
Source datasetuspto-grants-2005_05
ORD IDord-92b96563e7e440099c5a576f25baeec1
Source noteuspto-grants-2005_05