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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 516964Generated: October 26, 2026

Dichloromethane → 4-(4-Bromo-3-fluorobenzyl)morpholine

https://huagongshe.com/reaction/516964

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantMorpholineHCID 8083—
Reactant4-Bromo-3-fluorobenzaldehydeHCID 2783411—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
SolventDichloromethane methanolHCID 21226129—
ProductAmmoniaHCID 222—
Product4-(4-Bromo-3-fluorobenzyl)morpholineHCID 5341781866%

Reaction Conditions

Temperature59 °C

Reaction Steps

A mixture of morpholine (0.215 ml, 2.46 mmol) and 4-bromo-3-fluorobenzaldehyde, available from Alfa Aesar, (500 mg, 2.46 mmol) was prepared in chloroform (8 ml) at room temperature and heated to 58-60° C. in a sealed tube for 1 h. The mixture was then cooled to room temperature and sodium triacetoxyborohydride (783 mg, 3.69 mmol) was added and the mixture heated again to 58-60° C. in a sealed tube for 12 h. The mixture was then allowed to cool to room temperature, diluted with water (4 ml), shaken vigorously and the mixture filtered through a phase separator and the filtrate concentrated in vacuo. The mixture was then purified by SCX-2 chromatography (Eluent: dichloromethane (2×10 ml), 10% methanol/dichloromethane (2×10 ml), methanol (2×10 ml), 7M NH3 in methanol/dichloromethane (2×10 ml) to afford 4-(4-bromo-3-fluorobenzyl)morpholine as a colourless oil (447 mg, 1.63 mmol, 66%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115088B2
Source datasetuspto-grants-2015_08
ORD IDord-b04c39a32f78474e804a11fcc2e8dc71
Source noteuspto-grants-2015_08