HuagongsheHuagongshe Chemistry Print Report · For research reference only
(3-Trifluoromethylphenyl)urea → HCID 59684872, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (3-Trifluoromethylphenyl)urea | HCID 25712 | — |
| Reactant | 4-Cyanobenzaldehyde | HCID 66042 | — |
| Reactant | 1-Cyclobutylbutane-1,3-dione | HCID 55273563 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59684872 | HCID 59684872 | — |
Reaction Steps
To a stirred suspension of 1-cyclobutylbutane-1,3-dione (69 mg, 0.49 mmol), N-[3-(trifluoromethyl)phenyl]urea (100 mg, 0.49 mmol) and 4-cyanobenzaldehyde (64.2 mg, 0.49 mmol) in tetrahydrofuran (250 ml) is added polyphosphoric acid ethyl ester (300 mg). The reaction mixture is stirred at reflux for 18 hours. After cooling to room temperature, the solvent is removed in vacuo and the crude product is purified by preparative HPLC (RP18 column; eluent: acetonitrile/0.1% aq. formic acid 10:90→90:10).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08101615B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-915ba0e7758f4b4e93bc700ee8fae9f0 |
| Source note | uspto-grants-2012_01 |