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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1012231Generated: October 31, 2026

Triethylamine → 2-Amino-4-chlorophenylboronic acid pinacol ester

https://huagongshe.com/reaction/1012231

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4,4,5,5-Tetramethyl[1,3,2]dioxaborolaneHCID 2734768—
Reactant2-Bromo-5-chloroanilineHCID 11310276—
Solvent1,4-DioxaneHCID 31275—
Product2-Amino-4-chlorophenylboronic acid pinacol esterHCID 2315266667.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 2-bromo-5-chloroaniline (20.0 g, 96.9 mmol) in 1,4-dioxane (200 ml) were added triethylamine (54.0 ml, 487 mmol) and [1,1-bis(diphenylphosphino)ferrocene]dichloropalladium(II) dichloromethane complex (3.96 g, 4.84 mmol), and under a nitrogen stream, 4,4,5,5-tetramethyl-1,3,2-dioxaborolane (42.3 ml, 290 mmol) was added dropwise. The mixture was stirred at 100° C. for 10.5 hr. The mixture was allowed to cool to room temperature and filtered through celite. To the filtrate was added dropwise methanol (25 ml) at 0° C. The solvent was evaporated under reduced pressure, and the obtained residue was purified by silica gel chromatography (hexane:ethyl acetate=20:1) to give 5-chloro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenylamine (16.5 g, yield. 65%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977331B1
Source datasetuspto-grants-2011_07
ORD IDord-2c06441eb6154cab8b5b1e309bf8e7b9
Source noteuspto-grants-2011_07