HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Octene → HCID 67247774, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Octene | HCID 8125 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 9-Borabicyclo(3.3.1)nonane | HCID 78966 | — |
| Reactant | HCID 67247845 | HCID 67247845 | — |
| Reactant | HCID 178443689 | HCID 178443689 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67247774 | HCID 67247774 | — |
Reaction Steps
An octyl boronate intermediate is generated by adding 1-octene (1.38 g, 14.1 mmol) to a solution of 9-BBN in THF (28.3 mL of a 0.5 M solution, 14.1 mmol). The reaction mixture is stirred at room temperature overnight. An aqueous solution of sodium hydroxide (5.0 mL of a 3.0 M solution) is added, followed by the addition of compound 25 (3.10 g, 10.0 mmol) and Pd[P(Ph)3]4 (0.310 g, 0.270 mmol). The reaction is brought to reflux and maintained for 12 hours under an inert atmosphere. The reaction is cooled, filtered, concentrated in vacuo and the residue purified using silica gel chromatography with hexane/ethyl acetate (75:25) as solvent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07964649B2 |
| Source dataset | uspto-grants-2011_06 |
| ORD ID | ord-f3a36aeda49e45f3a2327786bc976811 |
| Source note | uspto-grants-2011_06 |