HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide dimethyl acetal → Ethyl 3-(dimethylamino)-2-isocyanoacrylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| Reactant | Ethyl isocyanoacetate | HCID 533707 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 3-(dimethylamino)-2-isocyanoacrylate | HCID 54355309 | — |
Reaction Steps
4-carboalkoxythiazoles are prepared essentially according to the procedure of Sch{umlaut over (of)}llkopf, U., Porsch, P., Lau, H. Liebigs Ann. Chem. 1444 (1979). Thus, according to Method 55 and 56, reaction of ethyl isocyanoacetate with N,N-dimethylformamide dimethyl acetal in a suitable alcoholic solvent such as ethanol at room temperature gives the corresponding 3-dimethylamino-2-isocyano-acrylic acid ethyl ester. A solution of this compound in a suitable solvent such as tetrahydrofuran is treated with gaseous hydrogen sulfide in the presence of a suitable tertiary amine base such as triethylamine or diiso-propylethylamine or the like at room temperature to give the corresponding 4-carboethoxy-thiazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06335350B1 |
| Source dataset | uspto-grants-2002_01 |
| ORD ID | ord-b4f56fdda0414aa4b937bb6e3874551e |
| Source note | uspto-grants-2002_01 |