HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetoacetanilide → Isoquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetoacetanilide | HCID 7592 | — |
| Reactant | Malononitrile | HCID 8010 | — |
| Product | Isoquinoline | HCID 8405 | 85% |
Reaction Steps
The procedure of Reference Example 5 was repeated except that 0.04 mole of acetoacetic anilide (Reference Example 8) or 0.04 mole of malononitrile (Reference Example 9) was employed instead of acetylacetone to give a corresponding isoquinoline derivative with yield of 85%, 65%, respectively. The structures of the obtained isoquinoline derivatives were identified by means of elementary analysis, IR spectrum and 1H-NMR spectrum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04515915 |
| Source dataset | uspto-grants-1985_05 |
| ORD ID | ord-72762389c1184c49931862144a7299b7 |
| Source note | uspto-grants-1985_05 |