Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748351Generated: October 27, 2026

3-Aminophenylboronic acid → 3-(1-trityl-1H-imidazol-4-yl)aniline

https://huagongshe.com/reaction/1748351

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Aminophenylboronic acidHCID 92269—
ReactantPotassium FluorideHCID 522689—
ReactantTri-tert-butylphosphine tetrafluoroborateHCID 2734635—
Reactant4-Bromo-1-trityl-1H-imidazoleHCID 2773274—
SolventTetrahydrofuranHCID 8028—
Product3-(1-trityl-1H-imidazol-4-yl)anilineHCID 1147511337.5%

Reaction Conditions

Temperature60 °C

Reaction Steps

(3-Aminophenyl)boronic acid (1.0 g, 7.3 mmol), 4-bromo-1-trityl-1H-imidazole (2.8 g, 7.3 mmol), tri-t-butylphosphonium tetrafluoroborate (424 mg, 1.5 mmol) and KF (1.4 g, 24.1 mmol) are added into dry THF (20 mL) and argon is bubbled through the mixture for 10 min. Tris-(dibenzylideneacetone)dipalladium(0) (669 mg, 0.7 mmol) is added and the reaction mixture is sealed and heated at 60° C. for 16 h. The solid is filtered and the filtrate is diluted with EtOAc (250 mL). The solution is washed with water (3×100 mL), brine (100 mL), dried (Na2SO4) and concentrated. The crude material is purified by flash column chromatography using methanol in CH2Cl2 to afford the title compound (1.1 g, 36%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150577B2
Source datasetuspto-grants-2015_10
ORD IDord-5b2fd438d4c34952a78e7f59bd411e6e
Source noteuspto-grants-2015_10