HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide dimethyl acetal → methyl (E)-5-(2-dimethylaminovinyl)-4-nitrothiophene-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| Reactant | Methyl 5-methyl-4-nitrothiophene-2-carboxylate | HCID 268679 | — |
| Product | methyl (E)-5-(2-dimethylaminovinyl)-4-nitrothiophene-2-carboxylate | HCID 12110978 | 96% |
Reaction Steps
A solution of methyl 4-nitro-5-methylthiophene-2-carboxylate (23 g, 114 mmol) in N,N-dimethylformamide dimethyl acetal (115 ml) was stirred at 110° C. for 1 hr. The reaction mixture was cooled to room temperature, concentrated under reduced pressure to about half amount, and poured into water (500 ml). The precipitated solid was collected by filtration, washed with water (500 ml×2), and dried under reduced pressure to give methyl (E)-5-(2-dimethylaminovinyl)-4-nitrothiophene-2-carboxylate (28 g, yield 96%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07659263B2 |
| Source dataset | uspto-grants-2010_02 |
| ORD ID | ord-a63ca5c3f36f4211ac99eb918c876544 |
| Source note | uspto-grants-2010_02 |