HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon tetrabromide → 3-(Bromomethyl)-2-methoxy-6-methylpyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | HCID 22678477 | HCID 22678477 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(Bromomethyl)-2-methoxy-6-methylpyridine | HCID 67253690 | 30.1% |
Reaction Steps
To a solution of (2-methoxy-6-methylpyridin-3-yl)methanol (4.7 g, 30.7 mmol) in dichloromethane (150 mL) was added triphenylphosphine (12.1 g, 46.0 mmol). The mixture was cooled in an ice bath with stirring under an atmosphere of nitrogen. Carbon tetrabromide (15.3 g; 46.0 mmol) was added and the mixture was stirred for 90 minutes. The mixture was concentrated under reduced pressure and purified using column chromatography on silica, eluting with dichloromethane/hexanes (1:1) to give 3-(bromomethyl)-2-methoxy-6-methylpyridine (2.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08841455B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-465f2463928a465a9694a89a9c7541e9 |
| Source note | uspto-grants-2014_09 |