HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-(Dibutylamino)thiophene-2-carbaldehyde → HCID 15508765, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-(Dibutylamino)thiophene-2-carbaldehyde | HCID 15396910 | — |
| Reactant | HCID 178448683 | HCID 178448683 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Product | HCID 15508765 | HCID 15508765 | — |
Reaction Steps
To a 100 ml flask, 3.0 g of 5-(dibutylamino)thiophene-2-carbaldehyde, 2.59 g of 1-butyl-6-hydroxy-4-methyl-2-oxo-1,2-dihydropyridine-3-carbonitrile and 10 ml of acetic anhydride are added, followed by heating while refluxing. After completion of the reaction, the resulting material is cooled and the solvent is removed to obtain (E)-1-butyl-5-((5-(dibutylamino)thiophen-2-yl)methylene)-4-methyl-2,6-dioxo-1,2,5,6-tetrahydropyridine-3-carbonitrile in solid phase.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09297940B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-fd093f580824459d9d900a240a39e9e4 |
| Source note | uspto-grants-2016_03 |