HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Bromobenzyl bromide → HCID 86729349, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Bromobenzyl bromide | HCID 69979 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 178418385 | HCID 178418385 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86729349 | HCID 86729349 | — |
Reaction Steps
To a solution of 1H-benzotriazole (0.52 g, 4.4 mmol) in THF (25 mL) was added potassium tert-butoxide (4.6 mL, 4.6 mmol, 1M in THF) followed by the addition of 1-bromo-3-(bromomethyl)benzene (1.0 g, 4.0 mmol). The solution was allowed to stir for 4 hours before the reaction was quenched with saturated aqueous NaHCO3 and diluted with EtOAc. The organic layer was separated and washed with brine, dried over anhydrous MgSO4, filtered, and concentrated to dryness in vacuo. The residue was purified by MPLC on silica gel (using a gradient elution of 0-80% EtOAc/hexanes) to afford the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08962608B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-4c8ae5a2d547428cb75bba9088d714f1 |
| Source note | uspto-grants-2015_02 |