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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1526892Erstellt: 26. Oktober 2026

2-(4-Bromophenyl)-1-morpholinoethanone → 4-(4-Bromophenethyl)morpholine

https://huagongshe.com/reaction/1526892

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-(4-Bromophenyl)-1-morpholinoethanoneHCID 875880—
EduktAluminium lithium hydrideHCID 21226445—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-(4-Bromophenethyl)morpholineHCID 1217780197%

Reaktionsbedingungen

Temperatur-30 °C

Reaktionsschritte

To a mixture of lithium aluminum hydride (3.35 g, 88.16 mmol, 2.00 equiv) in tetrahydrofuran (100 mL) maintained under nitrogen at −30° C. was added a solution of 2-(4-bromophenyl)-1-morpholinoethanone (12.5 g, 44.17 mmol, 1.00 equiv) in tetrahydrofuran (30 mL) dropwise with stirring. The reaction mixture was stirred at −30° C. for 30 min and then at room temperature for 2 h. The reaction was then quenched sequentially by the addition of 3.5 mL of water, 10 mL of 15% aqueous sodium hydroxide solution and 3.5 mL of water. The solid was removed by filtration. The filtrate was extracted with 1×150 mL of ethyl acetate. The organic layer was collected then washed with 2×30 mL of brine, dried over anhydrous sodium sulfate and concentrated under vacuum to give 11.5 g (97%) of 4-(4-bromophenethyl)morpholine as a white solid. LC-MS: (ES, m/z): 311 [M+CH3CN+H]+, 270 [M+H]+, 130, 102.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09085570B2
Quelldatensatzuspto-grants-2015_07
ORD IDord-277fc7f33c83419fb9e6423a597dbf60
Quellennotizuspto-grants-2015_07