HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 15442177, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | HCID 15442175 | HCID 15442175 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 15442177 | HCID 15442177 | — |
Reaction Steps
A mixture of tert-butyl 4-[(2-bromophenyl)carbamoyl]piperidine-1-carboxylate (8 mmol), benzylbromide (1.05 ml, 8.8 mmol) and Cs2CO3 (5.2 g, 16 mmol) in DMF (20 ml) is stirred at rt overnight. DMF is removed in vacuo and the residue is partitioned between H2O (40 ml) and EtOAc (40 ml). The layers are separated and the aqueous layer is extracted with EtOAc (20 ml). The combined extracts are washed with brine (20 ml), dried over Na2SO4 and evaporated. The residue is purified by flash column to give the title compound as a light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07851474B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-1d677c01067c45c9b1cae1ce525951ef |
| Source note | uspto-grants-2010_12 |