HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanogen Bromide → HCID 178482987, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 68644158 | HCID 68644158 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178482987 | HCID 178482987 | 28% |
Reaction Steps
N1-(3-Chloro-phenyl)-N1-methyl-propane-1,2,3-triamine (0.321 g, 1.5 mmol) was dissolved in tetrahydrofurane (5 ml) and potassium carbonate (0.249 g, 1.8 mmol) was added. Under cooling with an ice-bath a solution of cyanogen bromide (0.191 g, 1.8 mmol) in tetrahydrofurane (5 ml) was added dropwise. The cooling bath was removed and stirring was continued for one hour. Ethyl acetate (50 ml) and water (20 ml) were added and the organic layer was separated. The mixture was extracted again with ethyl acetate. The combined organic layers were dried over magnesium sulfate and evaporated. The residue was recrystallised from ethyl acetate to yield 0.1 g (28%) of a white solid; MS (ISP): 239.2 ((M+H)+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07812047B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-68896c109084470bb7632addfe745cd0 |
| Source note | uspto-grants-2010_10 |