HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Phenylprop-2-Enal → 5-(4-Phenyl-1,3-butadienyl)-1,2-dithiol-3-thione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Phenylprop-2-Enal | HCID 307 | — |
| Reactant | 3H-1,2-Dithiole-3-thione, 5-methyl- | HCID 137899 | — |
| Product | 5-(4-Phenyl-1,3-butadienyl)-1,2-dithiol-3-thione | HCID 53942573 | — |
Reaction Steps
In the same manner as in Example 1, a corresponding cinnamaldehyde derivative (i.e., 4-chloro-cinnamaldehyde, 4-methoxy-cinnamaldehyde, 4-dimethylamino-cinnamaldehyde, p-methyl-cinnamaldehyde, o-chloro-cinnamaldehyde or m-methyl-cinnamaldehyde) was reacted with 5-methyl-1,2-dithiol-3-thione to prepare the following compounds.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04760078 |
| Source dataset | uspto-grants-1988_07 |
| ORD ID | ord-8da12743090d4d08b19c9191b2d334a4 |
| Source note | uspto-grants-1988_07 |