HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Cyanoethanethioamide → HCID 178458231, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Cyanoethanethioamide | HCID 1416277 | — |
| Reactant | 4-(2-{[tert-Butyl(dimethyl)silyl]oxy}propoxy)benzaldehyde | HCID 59201970 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178458231 | HCID 178458231 | — |
Reaction Steps
A solution of 1.77 g (5.99 mmol) of the compound from Example 41A and 1.26 g (12.59 mmol) of cyanothioacetamide in 25 ml of ethanol is stirred at +78° C. for 6 h. The mixture is then cooled to RT and stirred at this temperature for a further 20 h. The resulting precipitate is filtered off with suction and washed with cold diethyl ether. Further product is obtained from the concentrated filtrate solution by chromatographic purification on silica gel 60 (mobile phase gradient cyclohexane/ethyl acetate 1:1→1:4).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08691850B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-e6df32c03e6e4fce828a081cf8247103 |
| Source note | uspto-grants-2014_04 |