HuagongsheHuagongshe Chemistry Print Report · For research reference only
Geranylacetone → (6S)-6,10-dimethylundecan-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Geranylacetone | HCID 1549778 | — |
| Reactant | (6S)-6,10-dimethylundecan-2-one | HCID 1551303 | — |
| Product | (6S)-6,10-dimethylundecan-2-one | HCID 1551303 | — |
| Product | (6R)-6,10-dimethylundecan-2-one | HCID 1715160 | — |
Reaction Steps
Specifically, it has been found that using the R-isomer of catalyst of formula (I) in the hydrogenation of E-geranyl acetone (=(E)-6,10-dimethylundeca-5,9-dien-2-one) the hydrogenation product (6S)-6,10-dimethylundecan-2-one is formed in more than 98% in respect to all of the possible stereoisomers (i.e. (6S)-6,10-dimethylundecan-2-one and (6R)-6,10-dimethylundecan-2-one) whereas the corresponding R-isomer is obtained only in amount of less than 2%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09181163B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-c711f65616254b5b8b3a3fb1c7350f12 |
| Source note | uspto-grants-2015_11 |