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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 516965Generated: October 30, 2026

Morpholine → 4-(4-Bromo-2,6-difluorobenzyl)morpholine

https://huagongshe.com/reaction/516965

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
Reactant4-Bromo-2,6-difluorobenzaldehydeHCID 2773290—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventChloroformHCID 6212—
Product4-(4-Bromo-2,6-difluorobenzyl)morpholineHCID 5939275837%

Reaction Conditions

Temperature59 °C

Reaction Steps

A mixture of 4-bromo-2,6-difluorobenzaldehyde, available from Sigma-Aldrich, (500 mg, 2.26 mmol) and morpholine (0.198 ml, 2.26 mmol) was prepared in chloroform (10 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 (719 mg, 3.39 mmol) was added and the mixture heated again to 58-60° C. in a sealed tube for 60 h. The mixture was allowed to cool down to room temperature and then washed with water (5 ml), filtered through a phase separator and concentrated in vacuo. Crude 1HNMR (CDCl3) suggested an 8:2 mixture of the desired amine to the imine product. After initial chromatography (1-5% methanol/dichloromethane) which did not separate products, mixture was purified by preparative HPLC to afford 4-(4-bromo-2,6-difluorobenzyl)morpholine as a colourless oil (247 mg, 0.85 mmol, 37%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115088B2
Source datasetuspto-grants-2015_08
ORD IDord-29cba3a5bfed4656ab314fc00e1531ad
Source noteuspto-grants-2015_08