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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 990528Generated: November 1, 2026

Morpholine → 3-Bromo-4-morpholinobenzaldehyde

https://huagongshe.com/reaction/990528

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Bromo-4-fluorobenzaldehydeHCID 173604—
SolventPyridineHCID 1049—
Product3-Bromo-4-morpholinobenzaldehydeHCID 2350602058.2%

Reaction Steps

To a pyridine (15 mL) solution of 3-bromo-4-fluorobenzaldehyde (1.0 g, 4.9 mmol) was added morpholine (0.5 mL, 5.7 mmol) and K2CO3 (0.69 g, 5.0 mmol), and the slurry was refluxed for 18 h. The solvent was removed, and the residue was partitioned between ethyl acetate and water. The organic layer was separated, dried (MgSO4) and evaporated to a yellow oil. Purification by flash chromatography on silica gel eluting with 15% ethyl acetate in hexane gave 0.77 g (58%) of the desired 3-bromo-4(4-morpholinyl)benzaldehyde product as an white solid. 1H NMR (CDCl3) δ3.18 (m, 4H), 3.90 (m, 4H), 7.10 (d, 1H), 7.78 (d, 1H), 8.07 (s, 1H), 9.83 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06458852B1
Source datasetuspto-grants-2002_10
ORD IDord-c61ce89182144b33a7014b260e3823db
Source noteuspto-grants-2002_10