HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Hexene → 2-Octanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Hexene | HCID 11597 | — |
| Reactant | Benzyl acetone | HCID 17355 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-Octanone | HCID 8093 | — |
Reaction Steps
Under the same reaction procedure and conditions as in Example 2 (tristriphenylphosphine rhodium (I) chloride 10 mol %, 150° C., 48 hours, toluene 100 mg), benzyl acetone 32 mg (0.22 mmol) and 1-hexene 182 mg (2.16 mmol) were reacted in the presence of various amounts of 2-amino-3-pycoline. A measurement was made of the yields of 2-octanone, and the results are given in Table 4, below. When 2-amino-3-pycoline was absent, 2-octanone was not obtained at all and benzyl acetone was recovered in its entirety.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06252118B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-7fb34858fd9b4e5a89bcb06df4ac4319 |
| Source note | uspto-grants-2001_06 |