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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 216703Erstellt: 25. Oktober 2026

Morpholine → (4-Bromo-2-fluorophenyl)(morpholino)methanone

https://huagongshe.com/reaction/216703

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMorpholineHCID 8083—
EduktOxalyl chlorideHCID 65578—
EduktDiisopropylethylamineHCID 81531—
Edukt4-Bromo-2-fluorobenzoic acidHCID 302681—
Edukt4-Bromo-2-fluorobenzoyl chlorideHCID 2734026—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
Produkt(4-Bromo-2-fluorophenyl)(morpholino)methanoneHCID 24705647—

Reaktionsschritte

A solution of 3.8 ml (44 mmol) oxalyl chloride in 30 ml CH2Cl2 is added dropwise to a iced-cooled solution of 4.88 g (21.9 mmol) 4-bromo-2-fluorobenzoic acid in 180 ml CH2Cl2. After complete addition, the cooling bath is removed and stirring maintained for 15 h at RT. The solvent is evaporated to dryness, the resultant colorless residue is dried under vacuum and then diluted with 80 ml CH2Cl2. This solution of 2-Fluoro-4-bromobenzoyl chloride (CAS 151982-51-3) is then added dropwise to a mixture of 9.55 ml (54.7 mmol) of diisopropylethylamine, 2.01 ml (23 mmol) of morpholine in 100 ml CH2Cl2. After 1 h 30, the reaction mixture is diluted with water and the two phases are separated. The aqueous phase is re-extracted with CH2Cl2 and the combined organic extracts are washed with water, saturated brine, dried over Na2SO4, filtered and the filtrate is concentrated in vacuo to afford, after drying in HV, the title compound which is used in the next step without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08193189B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-44bb9fc3e6a9466caf105c986df9a8e3
Quellennotizuspto-grants-2012_06