HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → α-[(Dimethylamino)methylene]-β-oxo-2-thiophenepropanenitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| Reactant | 5-(Thiophen-2-YL)-1,2-oxazole | HCID 12049986 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | α-[(Dimethylamino)methylene]-β-oxo-2-thiophenepropanenitrile | HCID 3743025 | 87.3% |
Reaction Steps
A mixture of 5-(2-thienyl)isoxazole (4.3 kg) and dimethylformamide dimethylacetal (6.1 kg; Lancaster) in toluene (12 L; Barton) is heated at reflux. As methanol forms it is removed by distillation. Solid forms from the reaction mixture. The reaction mixture is cooled and diluted with methyl-t-butyl ether (8 L; Van Waters). The precipitate is collected by filtration and washed with methyl-t-butyl ether (4 L). The solid is slurried with acetone (10 L; Batron) and hexanes (10 L; Mallinckrodt), then filtered and washed with hexanes (4 L). After drying in vacuo there is obtained 5.124 kg of α-[(dimethylamino)methylene]-β-oxo-2-thiophenepropane-nitrile (87% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06485746B1 |
| Source dataset | uspto-grants-2002_11 |
| ORD ID | ord-a974815b42cd49c39cfba72813295f17 |
| Source note | uspto-grants-2002_11 |