HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 5-(Bromomethyl)-1,2,3-trimethoxybenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Phosphorus tribromide | HCID 24614 | — |
| Reactant | 3,4,5-Trimethoxybenzyl alcohol | HCID 77449 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-(Bromomethyl)-1,2,3-trimethoxybenzene | HCID 10355271 | 202.8% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a solution of 3,4,5-trimethoxybenzyl alcohol (20.2 g, 0.108 mol) in 300 ml of dry tetrahydrofuran was added 4.12 ml (0.052 mol) of pyridine, and cooled to 0° C. A solution of phosphorous tribromide (4.8 ml, 0.051 mol) in 20 ml of dry tetrahydrofuran was added dropwise to the above solution at 0 ° C. The mixture was stirred for 1 hr. Tetrahydrofuran was concentrated. The residue was then diluted with 200 ml of 10% hydrochloric acid, and then extracted with 200 ml of ethyl acetate. The extract was dried over magnesium sulfate, filtered, concentrated, and dried in vacuum overnight. 3,4,5-Trimethoxybenzyl bromide (27 g, 100% yield) was obtained as a white solid, which can be used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05840991 |
| Source dataset | uspto-grants-1998_11 |
| ORD ID | ord-d81fec49ae5444638cd057f3f55b7c37 |
| Source note | uspto-grants-1998_11 |