HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1-(3-Bromophenyl)-3-heptyl-1-methylurea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | n-Heptyl isocyanate | HCID 138341 | — |
| Reactant | Benzenemethanamine, 3-bromo- | HCID 457587 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(3-Bromophenyl)-3-heptyl-1-methylurea | HCID 11616837 | 77% |
Reaction Steps
3.2 ml (20 mmol) of heptyl isocyanate are added to a solution of 2.5 g (13 mmol) of (3-bromophenyl)methyl-amine, thus prepared, in 10 ml of tetrahydrofuran in the presence of 2 ml of triethylamine. The reaction mixture is stirred at ambient temperature for 12 hours. The reaction is halted by the addition of 2 ml of water and then extracted with ethyl acetate. The organic phases are combined and dried over sodium sulphate. The solvents are evaporated and then the residue is purified by chromatography on a column of silica eluted with a heptane/ethyl acetate 70/30 mixture. 3.4 g (77%) of 1-(3-bromophenyl)-3-heptyl-1-methylurea are obtained in the solid form.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08357819B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-c5061c1d69ba4062942aad5a37dbd001 |
| Source note | uspto-grants-2013_01 |