HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Dibromopropane → 4-(3-Bromo-propyl)-morpholine-3,5-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Dibromopropane | HCID 8001 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Morpholine-3,5-dione | HCID 364836 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | 4-(3-Bromo-propyl)-morpholine-3,5-dione | HCID 59600132 | — |
Reaction Steps
A pale yellow suspension of morpholine-3,5-dione (1.2 g, 10 mmol), of 1,3-dibromopropane (3.4 ml, 33 mmol), and potassium carbonate (2.7 g, 19 mmol) in 23 ml of 2-butanone is refluxed under an argon athmosphere for 22 hours. After cooling, the suspension is concentrated on a rotary evaporator, poured into ice/water, and extracted twice with ethyl acetate. The combined organic phases are washed with brine, dried over anhydrous sodium sulphate, and evaporated. The residual yellow oil (2.06 g) is purified by chromatography (Biotage 40Mi, I=15 cm, cyclohexane/ethyl acetate 3:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07858781B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-e054adc19f6e4841ba991c1757f35a6e |
| Source note | uspto-grants-2010_12 |