HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → Methyl 4-nitro-5-[(E)-2-phenylethenyl]thiophene-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | Methyl 5-methyl-4-nitrothiophene-2-carboxylate | HCID 268679 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 4-nitro-5-[(E)-2-phenylethenyl]thiophene-2-carboxylate | HCID 11514785 | 67% |
Reaction Steps
A solution (0.33 M) of methyl 5-methyl-4-nitrothiophene-2-carboxylate in MeOH, was treated with benzaldehyde (1.5 eq.). The reaction mixture was heated to reflux and when it became a clear solution a catalytic amount of pyrrolidine (0.01 eq.) was added. After 18 h at reflux additional pyrrolidine (0.01 eq.) was added. The reaction was heated to reflux for 40 h. After cooling down, evaporation of the solvent gave a residue that was purified by flash chromatography on silica gel (1:9 AcOEt/petroleum ether) to afford the title compound (67%) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07781431B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-0dbdf03c2e934233833547dbb1506e68 |
| Source note | uspto-grants-2010_08 |