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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 882965Generated: October 25, 2026

1,2-Dichloroethane → (4-Bromo-3-fluorophenyl)(morpholin-4-yl)methanone

https://huagongshe.com/reaction/882965

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantEthylmorpholineHCID 7525—
ReactantMorpholineHCID 8083—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant4-Bromo-3-fluorobenzoic acidHCID 2773341—
SolventDimethylformamideHCID 6228—
Product(4-Bromo-3-fluorophenyl)(morpholin-4-yl)methanoneHCID 4847411598.5%

Reaction Steps

A 500 mL flask was charged with 4-bromo-3-fluorobenzoic acid (5.00 g, 22.83 mmol), 100 mL DMF, morpholine (2.4 ml, 27.5 mmol), and 4-Ethylmorpholine (8.6 ml, 67.9 mmol). HOBt (4.32 g, 32.0 mmol) was added followed by EDC (5.25 g, 27.4 mmol) and the reaction allowed to stir at room temperature for 18 hours. The reaction was concentrated and the resulting orange syrup taken up in 100 mL EtOAc and 100 mL water. The organic layer was washed with 100 mL 2N HCl, 100 mL saturated sodium bicarbonate, and 100 mL saturated sodium chloride. The organic was then dried with MgSO4, filtered, and concentrated to give 6.476 g (98%) of a viscous yellow oil. This material was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08236799B2
Source datasetuspto-grants-2012_08
ORD IDord-77d51c2daee940da81507bf578f69cff
Source noteuspto-grants-2012_08