HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → Benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Octanal | HCID 454 | — |
| Product | Benzaldehyde | HCID 240 | — |
| Product | Octanal | HCID 454 | — |
| Product | 2-(Phenylmethylene)octanal | HCID 7585 | — |
Reaction Steps
The conversion of the benzaldehyde (bald) amounted to 65.6% and the degree of conversion of octanal to 100%. The selectivities of benzaldehyde and octanal to give α-hexylcinnamaldehyde (α-hex) were 94.9% and 96.2%, respectively, while the selectivity of octanal to give α-hexyldecenal (α-HD) was 1.0%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05728892 |
| Source dataset | uspto-grants-1998_03 |
| ORD ID | ord-c24b8279498c4f1780da6e8b6f498cbc |
| Source note | uspto-grants-1998_03 |