HuagongsheHuagongshe Chemistry Print Report · For research reference only
Morpholine → 2-Bromo-1-(morpholin-4-yl)ethan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-Bromo-1-(morpholin-4-yl)ethan-1-one | HCID 13996876 | 45% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06878706B1 |
| Source dataset | uspto-grants-2005_04 |
| ORD ID | ord-31900f8da4cd407aa7a8e4319587aabb |
| Source note | uspto-grants-2005_04 |