HuagongsheHuagongshe Chemistry Print Report · For research reference only
Propanal → HCID 15907301, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Propanal | HCID 527 | — |
| Reactant | 2-Methyl-3-phenylpropionaldehyde | HCID 95593 | — |
| Product | HCID 15907301 | HCID 15907301 | — |
Reaction Steps
The 2,4-dimethyl-5-phenylpentan-1-yl derivatives in accordance with the present invention can be prepared by a variety of ways. For example, by an Aldol condensation between 2-methyl-3-phenylpropanal and proprionaldehyde, followed by hydrogenation of the resulting α,β-unsaturated aldehyde to form the saturated aldehyde, 2,4-dimethyl-5-phenylpentanal as described above. This aldehyde is the direct precursor for the alcohol, 2,4-dimethyl-5 -phenylpentan-1-ol via reduction with, e.g. sodium borohydride, as well as the nitrile, 2,4-dimethyl-5-phenyl-pentanitrile via oxidation dehydration chemistry by reaction of hydroxylamine/formic acid as described above.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06310033B1 |
| Source dataset | uspto-grants-2001_10 |
| ORD ID | ord-578a6baab8d24ddb9513a57398022870 |
| Source note | uspto-grants-2001_10 |