HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phosphorus tribromide → 1-(Bromomethyl)-2,3,5-triiodobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phosphorus tribromide | HCID 24614 | — |
| Reactant | 2,3,5-Triiodobenzyl alcohol | HCID 3495743 | — |
| Reactant | Water methylene chloride | HCID 21908982 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(Bromomethyl)-2,3,5-triiodobenzene | HCID 53403077 | 85.2% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
A solution of phosphorous tribromide (3.8 ml, 40 mmol) was added dropwise to a solution of 2,3,5-triiodobenzyl alcohol 1 (9.72 g, 20 mmol) in dry tetrahydrofuran (50 ml) at 0° C. under dry nitrogen gas flow. The reaction mixture was stirred 5 minutes at 0° C., then 20 minutes at room temperature (18° C.), then cold H2O/DCM (60/60 ml) was added. The resulting aqueous phase was extracted with dichloromethane (2×10 ml). The combined organic extracts were washed with NaHCO3aq (20 ml) and H2O (20 ml) then dried (Na2SO4), filtered and concentrated. The white solid was also washed with cold methanol (45 ml). 9.35 g of 2,3,5-triiodobenzyl bromide in the form of a white clean solid was obtained in 85% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09115230B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-94c41136f17a4dfcbbc47ce7d429f690 |
| Source note | uspto-grants-2015_08 |