HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Nitroacetophenone → (2E)-3-(dimethylamino)-1-(4-nitrophenyl)prop-2-en-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Nitroacetophenone | HCID 7487 | — |
| Reactant | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| Product | (2E)-3-(dimethylamino)-1-(4-nitrophenyl)prop-2-en-1-one | HCID 1475992 | — |
Reaction Steps
A solution of 1-(4-nitrophenyl)ethanone (2.2 g, 13 mmol) and N,N-dimethylformamide dimethyl acetal (25 ml) was heated to 120° C. in a sealed tube overnight. The volatiles were removed. The residue was dissolved in DCM and washed twice with H2O. The DCM layer was dried with MgSO4. The crude product was purified by flash chromatography (silica gel, 100% EtOAc) to isolate (E)-3-(dimethylamino)-1-(4-nitrophenyl)prop-2-en-1-one (2.2 g,) as a yellow solid. 1H NMR (400 MHz, CDCl3) δ 2.99 (s, 3H), 3.23 (s, 3H), 5.70 (d, J=12.4 Hz, 1H), 7.94 (d, J=12.4 Hz, 1H), 8.03 (m, 2H), 8.26 (m, 2H). MS (ESI): 221 (M+H+)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08491869B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-f2faeee14eb44263a555d952cecfd0a1 |
| Source note | uspto-grants-2013_07 |