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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1874003Generated: October 31, 2026

Morpholine → 3-Fluoro-4-(morpholine-4-carbonyl)phenylboronic acid

https://huagongshe.com/reaction/1874003

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
Reactant4-Carboxy-3-fluorophenylboronic acidHCID 2763201—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
SolventDimethylformamideHCID 6228—
Product3-Fluoro-4-(morpholine-4-carbonyl)phenylboronic acidHCID 5761841590%

Reaction Steps

A solution of 4-borono-2-fluorobenzoic acid (1.000 g, 5.44 mmol), morpholine (0.951 mL, 10.87 mmol) and O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (2.103 g, 5.53 mmol) in DMF (10 mL) was stirred at room temperature for 16 h and quenched with 1 N HCl (20 mL). Attempted extraction with EtOAc did not remove all of the product from aqueous phase. The two phases were combined, concentrated and purified by reverse phase HPLC (Sunfire S10 30×250 mm column, 30-45% solvent B gradient) to give the expected product as white solid (1.2385 g, 90% yield). MS (ES+) m/z: 254 (M+H); LC retention time: 2.06 min (analytical HPLC Method A).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304539B2
Source datasetuspto-grants-2012_11
ORD IDord-494752a6a5fe4662afb92f94c6b449f5
Source noteuspto-grants-2012_11