HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon tetrabromide → (6-Bromohexyl)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 6-Phenyl-1-hexanol | HCID 520110 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (6-Bromohexyl)benzene | HCID 561788 | — |
Reaction Steps
A solution of 6-phenylhexanoic acid (19.8 mmoles in sieve dried tetrahydrofuran (5 ml) was reduced with diborane in tetrahydrofuran (30 ml, 29.1 mmoles) at 0° C. for 4 hours to give 6-phenylhexanol. To an ice cold solution of the hexanol (ca. 19.8 mmoles) and carbon tetrabromide (21.98 mmoles) in methylene chloride (50 ml) was added triphenylphosphine (22.30 mmoles) in methylene chloride (50 ml) and the resultinq solution was stirred for 2.5 hours. The volatiles were evaporated and the residue was taken up in ether (100 ml), cooled in ice, and filtered. The filtrate was evaporated and distilled to afford 6-phenylhexyl bromide as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04937253 |
| Source dataset | uspto-grants-1990_06 |
| ORD ID | ord-be5ae2a470cf4021b0a267d8e52d2b50 |
| Source note | uspto-grants-1990_06 |