HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 4-nitrobutyrate → HCID 717405, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 4-nitrobutyrate | HCID 25604 | — |
| Reactant | 4-(Trifluoromethyl)benzaldehyde | HCID 67996 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 717405 | HCID 717405 | — |
Reaction Steps
Ammonium acetate (21.21 g), 4-trifluoromethylbenzaldehyde (19.61 ml) and methyl 4-nitrobutyrate (17.5 ml) in ethanol (150 ml) was stirred and heated under reflux for 3.5 h. After cooling to room temperature, an orange solid was formed which was filtered, washed with ethanol (2×100 ml) and dried in vacuo to give the title compound (30.56 g). Mass spectrometry. For C12H11F3N2O3, m/z 5.77 (2M+H+), 306 (M+NH4), 289 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05703240 |
| Source dataset | uspto-grants-1997_12 |
| ORD ID | ord-eb0f1bc7c164472cb38d052245e3adf0 |
| Source note | uspto-grants-1997_12 |