HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanamide → HCID 23525769, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanamide | HCID 9864 | — |
| Reactant | 3-Fluorophenacyl bromide | HCID 2737451 | — |
| Reactant | HCID 23525774 | HCID 23525774 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 23525769 | HCID 23525769 | — |
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 19, 306 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 (TCl, 216 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, 480 mg, 99%. MS (ES) MH+=485.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06818663B2 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-a24326752aea4e4aa3772697a57c8b59 |
| Source note | uspto-grants-2004_11 |