HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 118691670, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | (3-Trifluoromethylphenyl)urea | HCID 25712 | — |
| Reactant | Acetylacetone | HCID 31261 | — |
| Reactant | 3-Bromo-4-formylbenzonitrile | HCID 20510518 | — |
| Product | HCID 118691670 | HCID 118691670 | — |
Reaction Steps
3-Bromo-4-formyl-benzonitrile (intermediate 2, 3.25 g, 14.7 mmol) is stirred with acetylacetone (2.42 mL, 19.1 mmol), 3-(trifluoromethyl)phenylurea (3 g, 14.7 mmol) and polyphosphoric acid (3.02 g, 7.90 mmol) in tetrahydrofurane (80.0 mL) at 60° C. for 48 h. The reaction mixture is concentrated in vacuo and ethyl acetate and water is added and the phases are separated. The aqueous phase is extracted twice with ethyl acetate. The combined organic phases are washed with saturated sodium chloride solution, dried over MgSO4 and concentrated. Yield: 7.66 g; ESI mass spectrum: [M+H]+=508; Retention time HPLC: 1.14 min (HPLC method Z018_S04)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09290457B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-cb420192d38049d8895278f357d0a251 |
| Source note | uspto-grants-2016_03 |