HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon tetrabromide → cis 4-(2-Fluoro-5-bromobenzyloxy)but-2-enyl bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 4-(2-Fluoro-5-bromobenzyloxy)but-2-en-1-ol | HCID 54380840 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | cis 4-(2-Fluoro-5-bromobenzyloxy)but-2-enyl bromide | HCID 59958660 | — |
Reaction Steps
In a 100 ml round bottom flask 4-(2-fluoro-5-bromobenzyloxy)but-2-en-1-ol (2.145 g, 7.80 mmol) was dissolved in diethyl ether under a nitrogen atmosphere. Triphenylphosphine (2.66 g, 10.1 mmol) and then carbon tetrabromide (3.36 g, 10.1 mmol) were added to the reaction mixture. The resulting mixture was stirred for six hours at ambient temperature. A white precipitate formed during the stirring. The progress of the reaction was monitored by thin layer chromatography. The solution was filtered and the filtrate was evaporated to give a thick oil. The desired title intermediate was further purified by liquid chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06245761B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-e41262f4ca1147f9a33952c021ccada0 |
| Source note | uspto-grants-2001_06 |