HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Cinnamoylbenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 6-Methoxypyridine-3-carbaldehyde | HCID 3364576 | — |
| Reactant | 1-(2-hydroxy-4-(methoxymethoxy)phenyl)ethanone | HCID 11745559 | — |
| Product | Cinnamoylbenzene | HCID 7189 | 34% |
Reaction Steps
4.18 g (21.3 mmol) of 1-(2-hydroxy-4-(methoxymethoxy)phenyl)ethanone, 2.8 g of 6-methoxy-3-pyridine-carboxaldehyde (20.4 mmol), and 1.8 g (32.1 mmol) of KOH were reacted in 60 ml of EtOH and 20 ml of H2O ml to give 2.18 g (34%) of chalcone after purification. 1H NMR (300 MHz, CDCl3): δ 13.27 (s, 1H), 8.42 (d, J=2.4 Hz, 1H), 7.95-7.82 (m, 3H), 7.50 (d, J=15.6 Hz, 1H), 6.83 (d, J=8.7 Hz, 1H), 6.67 (d, J=2.7 Hz, 1H), 6.61 (d, d, J=2.4, 9.0 Hz, 1H), 5.25 (s, 2H), 4.02 (s, 3H), 3.51 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08449936B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-029da9ad888f4ee9a024859bc55cea33 |
| Source note | uspto-grants-2013_05 |