Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2180358Generated: October 30, 2026

P-Anisidine → HCID 10729720, compound

https://huagongshe.com/reaction/2180358

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-AnisidineHCID 7732—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant1-Bromo-4-tert-butylbenzeneHCID 77595—
ReactantSodium t-butoxideHCID 23676156—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventDiethyl EtherHCID 3283—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventDodecaneHCID 8182—
ProductHCID 10729720HCID 107297205.5%

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), 1-bromo-4-tert-butylbenzene (86 μL, 0.5 mmol), and p-anisidine (74 mg, 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 7 mg of the desired product (which was used for calibration with the internal standard). The GC yield was calculated to be 12%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06888029B2
Source datasetuspto-grants-2005_05
ORD IDord-f18d945034884926a42523e74814507f
Source noteuspto-grants-2005_05