HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl bromomalonate → HCID 178470560, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl bromomalonate | HCID 69637 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Thiourea, [2-(trifluoromethyl)phenyl]- | HCID 737227 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178470560 | HCID 178470560 | — |
Reaction Steps
To a stirred solution of 2-(trifluoromethyl)phenylthiourea (Menai Organics, 2.36 g, 10.7 mmol), Hunig's base (Aldrich, 1.9 mL, 10.7 mmol) in EtOH (10 mL) was added diethyl bromomalonate (2.0 mL, 10.7 mmol). After 1.5 h at room temperature, the reaction mixture was diluted with EtOAc, washed with saturated NaHCO3 and brine, dried over Na2SO4, filtered, and concentrated in vacuo. The crude product was purified by silica gel chromatography. MS: 333 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07807700B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-778c2f52c6ca40d59a23c32dcb67baff |
| Source note | uspto-grants-2010_10 |