HuagongsheHuagongshe Chemistry Print Report · For research reference only
alpha-Hydroxyacetophenone → Cinnamoylbenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | alpha-Hydroxyacetophenone | HCID 68490 | — |
| Reactant | 4-Morpholinobenzaldehyde | HCID 291349 | — |
| Reactant | HCID 178418582 | HCID 178418582 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Cinnamoylbenzene | HCID 7189 | 83.5% |
Reaction Steps
2.15 g (15.8 mmol) of 2-hydroxyacetophenone, 2.8 g of 4-morpholinobenzaldehyde (14.5 mmol), and 10 ml of 25% wt NaOCH3 were reacted in 50 ml of dry THF to give 2.52 g (56%) of chalcone after purification. 1H NMR (300 MHz, CDCl3): δ 12.99 (s, 1H), 8.43 (d, J=2.4 Hz, 1H), 7.93-7.84 (m, 3H), 7.52-7.48 (m, 2H), 7.03 (d, d, J=0.9, 8.4 Hz, 1H), 6.97-6.92 (m, 1H), 6.68 (d, J=9.0 Hz, 1H), 3.86-3.83 (m, 4H), 3.69-3.66 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08449936B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-3d34b574710b4d48aebe7f49add191d3 |
| Source note | uspto-grants-2013_05 |