HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon tetrabromide → 1-(Bromomethyl)-2-fluoro-3-methoxybenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-Fluoro-3-methoxybenzyl alcohol | HCID 593589 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(Bromomethyl)-2-fluoro-3-methoxybenzene | HCID 26986100 | — |
Reaction Steps
Triphenylphosphine (11.1 g) was added to a solution of the subtitle product of step ii) (5.0 g) in DCM (200 ml) followed by the portionwise addition of carbon tetrabromide (14.0 g). The reaction was stirred for 4 h before the addition of further triphenylphosphine (2.0 g) and carbon tetrabromide (2.0 g) and stirring maintained for 1 h. The mixture was concentrated to 30 ml volume and diluted in Et2O (300 ml). The solid precipitate was filtered and washed with Et2O (3×) and the filtrate concentrated in vacuo. The residue was purified by column chromatography (10% Et2O/iso-hexane) to afford the subtitle compound as a clear oil. Yield: 5.2 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07582644B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-9f802557b38140a28afce8dfa93633d6 |
| Source note | uspto-grants-2009_09 |