HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron tribromide → 3-Bromo-4-fluorobenzyl Bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | 3-Bromo-4-fluorobenzyl Alcohol | HCID 2773351 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Bromo-4-fluorobenzyl Bromide | HCID 12922710 | — |
Reaction Steps
(3-Bromo-4-fluorophenyl)methanol (0.264 g, 1.29 mmol) was dissolved in DCM (3 mL). The solution was cooled to 0 deg, and tribromoborane (1.0 M in DCM, 0.863 ml, 0.863 mmol) was added. The mixture was stirred at 0 deg for 1 h, then rt for 1 h. The reaction was quenched with water, and the mixture was transferred to a separatory funnel with half-saturated NaHCO3 (15 mL), and the aqueous phase was extracted with DCM (3×20 mL). The organics were combined, washed with half-saturated brine (5 mL), dried over sodium sulfate and concentrated. Purification of the residue through silica gel (40 mL) using 5% EtOAc-hexane afforded the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07745484B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-bdee873a287547a4bb709c42021939a4 |
| Source note | uspto-grants-2010_06 |