HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 4-(4-Amino-3-bromo-phenyl)-1-methyl-piperidine-2,6-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 4-(4-Amino-phenyl)-1-methyl-piperidine-2,6-dione | HCID 59771129 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(4-Amino-3-bromo-phenyl)-1-methyl-piperidine-2,6-dione | HCID 59771219 | 67% |
Reaction Steps
A solution of 289 mg (1.32 mmol) of 4-(4-amino-phenyl)-1-methyl-piperidine-2,6-dione (as prepared in the previous step) in CH2Cl2 (15 mL) was treated portionwise with 224 mg (1.29 mmol) of solid NBS for 20 min. The mixture was diluted with CH2Cl2 (30 mL) and washed with saturated aqueous NaHCO3 (2×30 mL). The organic layer was dried (MgSO4) and concentrated in vacuo. Silica gel chromatography of the residue with 25-50% EtOAc-hexane afforded 265 mg (67%) of the title compound as a tan solid: Mass spectrum (ESI, m/z): Calcd. for C12H13N2O2Br, 297.0/299.0 (M+H), found 297.0/299.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07973035B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-ada8d1be29fd44b5990d5661f9bf2fd4 |
| Source note | uspto-grants-2011_07 |