HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorobis((1S,2R,3S,5S)-2,6,6-trimethylbicyclo(3.1.1)hept-3-yl)borane → (R)-1-(4-isobutylphenyl)pentan-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorobis((1S,2R,3S,5S)-2,6,6-trimethylbicyclo(3.1.1)hept-3-yl)borane | HCID 9923113 | — |
| Reactant | 4'-Isobutylpentanophenone | HCID 10998490 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (R)-1-(4-isobutylphenyl)pentan-1-ol | HCID 11074925 | 30% |
Reaction Steps
4'-Isobutylpentanophenone (2.1 g) was added to a solution of (+)-B-chlorodiisopinocampheylborane (3.57 g) in tetrahydrofuran (7 ml) at -25° C. After stirring for 5 hours, the solvent was removed and the residue was dissolved in ethyl ether (30 ml). To this solution was added diethanolamine (2 ml), and the mixture was stirred for 2 hours. The solid was filtered off and washed with ethyl ether. The combined filtrates were concentrated and the residue was chromatographed on silica gel (hexane:dichloromethane =1:2) to give (R)-1-(4-isobutylphenyl)pentan-1-ol (635 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05312829 |
| Source dataset | uspto-grants-1994_05 |
| ORD ID | ord-2f76a18addf04736869fc8be51318c07 |
| Source note | uspto-grants-1994_05 |