HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 4-(3-t-butylureidomethyl)-1-(N-heptylaminomethyl)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Iodoheptane | HCID 20274 | — |
| Reactant | 4-(3-t-Butylureidomethyl)-1-aminomethylbenzene | HCID 20096740 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(3-t-butylureidomethyl)-1-(N-heptylaminomethyl)benzene | HCID 20096726 | 47.4% |
Reaction Steps
A mixture of 0.97 g 4-(3-t-butylureidomethyl)-1-aminomethylbenzene obtained in Example 8, 0.57 g anhydrous potassium carbonate and 20 ml dimethylformamide was stirred at room temperature for 30 minutes, 0.93 g 1-iodoheptane was added, and stirring was continued at room temperature for an additional three hours. After distilling off the solvent under reduced pressure, the residue was extracted with chloroform, and the extract was washed with water. The chloroform was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography, giving 0.65 g of 4-(3-t-butylureidomethyl)-1-(N-heptylaminomethyl)benzene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05384425 |
| Source dataset | uspto-grants-1995_01 |
| ORD ID | ord-9a269102a0694b1dbe9ae00c8240a19b |
| Source note | uspto-grants-1995_01 |