HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanamide → HCID 60063784, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanamide | HCID 9864 | — |
| Reactant | 3-Fluorophenacyl bromide | HCID 2737451 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 60063757 | HCID 60063757 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 60063784 | HCID 60063784 | — |
Reaction Steps
Cyanamide (46.2 mg, 1.1 mmol) was suspended in acetonitrile (5 mL). To the stirred suspension, potassium tert-butoxide (123 mg, 1.1 mmol) in 2 mL of tert-butanol was added followed by isothiocyanate (Example 1, 334 mg, 1 mmol). The mixture was stirred for 30 minutes at room temperature followed by the addition of 2-bromo-1-(3-fluoro-phenyl)-ethanone (TCI, 261 mg, 1 mmol). After being stirred for 2 hours at room temperature, the mixture was poured into water and the new mixture was extracted with ether. The extract was dried(Na2SO4) and concentrated to give the desired product as a yellow solid, 510 mg, 99%. MS (ES) MH+=513.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06818663B2 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-0e2a9dc9df77488c87f7fb281a9a446e |
| Source note | uspto-grants-2004_11 |