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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354436Generated: October 31, 2026

Water → (4-Bromo-3-fluorophenyl)(morpholin-4-yl)methanone

https://huagongshe.com/reaction/2354436

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMorpholineHCID 8083—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant4-Bromo-3-fluorobenzoic acidHCID 2773341—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product(4-Bromo-3-fluorophenyl)(morpholin-4-yl)methanoneHCID 4847411566%

Reaction Steps

To a room temperature solution containing 10 g of 4-bromo-3-fluorobenzoic acid (45.7 mmols) in 228 mL of dichloromethane was added 1.67 g of DMAP (13.7 mmols), 11.3 g of EDCI (59.2 mmols), and 5.11 mL of morpholine (59.4 mmols). After stirring at ambient temperature for 18 h, 20 mL of water was added to the reaction mixture. The layers were separated, and the organic layer was washed with water (3×20 mL), dried over MgSO4, and filtered through a frit. The resulting solution was concentrated to a pale yellow oil which was purified by silica gel chromatography (120 g redisep column, silica 40 um, 60 A, 85 ml/min, A: EtOAc, B: hexanes, A: 50% for 5 min, then 50-70% for 8 min) to give 8.62 g (66%) of title compound as a yellow oil. MS (ES) m/e 288 [M+]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07749998B2
Source datasetuspto-grants-2010_07
ORD IDord-9524a70de2f749cdbbc3dacf1c61a808
Source noteuspto-grants-2010_07