HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromobenzyl bromide → 2-(But-3-en-1-yl)bromobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromobenzyl bromide | HCID 76965 | — |
| Reactant | HCID 178455850 | HCID 178455850 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(But-3-en-1-yl)bromobenzene | HCID 3485712 | — |
Reaction Steps
To an ice cold solution of 2-bromobenzyl bromide (5.00 g, 0.020 mol) in THF (25 mL) was added 1M allyl magnesium bromide (100 mL, 0.100 mol) slowly via cannula. The reaction mixture was stirred at reflux for 1.5 h, cooled in an ice bath and quenched with 50 mL of aqueous 2M H2SO4. Water (50 mL) was added to dissolve any remaining solid and the layers were separated. The aqueous layer was extracted with Et2O (2×150 mL). The combined organic extracts Were dried over Na2SO4, filtered and concentrated to yield 1-bromo-2-but-3-enyl-benzene as a light yellow oil. The isolated crude product was carried forward without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07053101B2 |
| Source dataset | uspto-grants-2006_05 |
| ORD ID | ord-ed0ffa8b47004e11a7fec2e6b4636536 |
| Source note | uspto-grants-2006_05 |