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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814732Generated: October 30, 2026

Morpholine → 2-Bromo-1-(morpholin-4-yl)ethan-1-one

https://huagongshe.com/reaction/1814732

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantBromoacetyl bromideHCID 61147—
SolventDiethyl EtherHCID 3283—
Product2-Bromo-1-(morpholin-4-yl)ethan-1-oneHCID 1399687645%

Reaction Steps

Bromoacetyl bromide (6.0 mL, 68.9 mmol) was dissolved in 30 mL of ether. Morpholine (7.0 mL, 80.3 mmol) was added dropwise to the above solution at −78° C. The reaction mixture was warmed to room temperature in 30 min. The resulting white solid was removed by filtration and washed with ether. The filtrate was washed with saturated sodium bicarbonate (20 mL×2). The combined aqueous phase was extracted with ether (20 mL×4). The combined organic extracts were washed with brine and dried over sodium sulfate. The solvent was removed in vacuo to give N-bromoacetyl-morpholine (3.73 g, 45%) as a clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06878706B1
Source datasetuspto-grants-2005_04
ORD IDord-31900f8da4cd407aa7a8e4319587aabb
Source noteuspto-grants-2005_04