HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Cyanoethanethioamide → HCID 178510482, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Cyanoethanethioamide | HCID 1416277 | — |
| Reactant | [4-(2-Azidoethoxy)benzylidene]malononitrile | HCID 86624335 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178510482 | HCID 178510482 | — |
Reaction Steps
A solution of 2.39 g (9.98 mmol) of the compound from Example 37A and 2.50 g (24.92 mmol) of cyanothioacetamide in 100 ml of ethanol is stirred at +78° C. for 6 h. After cooling to RT and a further 12 h of standing without stirring, the reaction mixture is concentrated using a rotary evaporator. The residue is recrystallized from about 30 ml of ethanol. The resulting precipitate is filtered off with suction and washed twice with in each case 10 ml of methyl tert-butyl ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08691850B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-b01065bebd994833b94fcaac08b370c1 |
| Source note | uspto-grants-2014_04 |