HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyrrolidine → HCID 58679079, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | Methyl 5-methyl-4-nitrothiophene-2-carboxylate | HCID 268679 | — |
| Reactant | 2,4-Bis(benzyloxy)benzaldehyde | HCID 1809080 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 58679079 | HCID 58679079 | 82.3% |
Reaction Steps
To a solution of methyl 4-nitro-5-methylthiophene-2-carboxylate (1.50 g, 7.46 mmol) in ethanol (7.5 ml) were added 2,4-bisbenzyloxybenzaldehyde (2.49 g, 7.83 mmol) and pyrrolidine (0.65 ml, 7.83 mmol). After stirring for 1 hr with heating under reflux, the reaction mixture was allowed to cool to room temperature. The precipitated solid was collected by filtration. The solid was washed with ethanol (3 ml×3), and dried under reduced pressure to give methyl (E)-5-[2-(2,4-bisbenzyloxyphenyl)vinyl]-4-nitrothiophene-2-carboxylate (3.08 g, yield 82%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07659263B2 |
| Source dataset | uspto-grants-2010_02 |
| ORD ID | ord-cdc63fbfca894cc4bccaf77020631e05 |
| Source note | uspto-grants-2010_02 |