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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1674755Generated: November 1, 2026

Triphenylphosphine → 4-(2-Morpholin-4-ylethoxy)benzeneboronic acid, pinacol ester

https://huagongshe.com/reaction/1674755

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant2-MorpholinoethanolHCID 61163—
Reactant4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenolHCID 2734624—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
SolventDichloromethaneHCID 6344—
Product4-(2-Morpholin-4-ylethoxy)benzeneboronic acid, pinacol esterHCID 462591074%

Reaction Steps

To a stirring solution of 4-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)-phenol (2.55 g, 11.58 mmol), 2-morpholin-4-ylethanol (1.60 mL, 1.73 g, 13.2 mmol) and triphenyl phosphine (3.64 g, 13.9 mmol) in methylene chloride (60 mL) at 0° C. was added dropwise DIAD (2.82 g, 13.9 mmol). The reaction was allowed to warm to room temperature and stir overnight. After 18 hours, additional portions of triphenyl phosphine (1.51 g, 5.8 mmol), 2-morpholin-4-ylethanol (0.70 mL, 5.8 mmol), and DIAD (1.17 g, 5.8 mmol) were added. After stirring an additional 2 hours at room temperature the reaction was concentrated and the residue purified by flash chromatography (5% to 25% EtOAc in CHCl3) to provide the product as a white solid (2.855 g, 74%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003641B2
Source datasetuspto-grants-2011_08
ORD IDord-d4b41ae8371a46cfb4075dd933908ef7
Source noteuspto-grants-2011_08