HuagongsheHuagongshe Chemistry Print Report · For research reference only
alpha-Hydroxyacetophenone → Cinnamoylbenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | alpha-Hydroxyacetophenone | HCID 68490 | — |
| Reactant | 4,5-Dimethyl-2-furaldehyde | HCID 643406 | — |
| Reactant | HCID 178418582 | HCID 178418582 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Cinnamoylbenzene | HCID 7189 | 58.2% |
Reaction Steps
2.0 g (14.7 mmol) of 2-hydroxyacetophenone, 1.75 g of 4,5-dimethylfuran-2-carbaldehyde (14.1 mmol), and 10 ml of 25% wt NaOCH3 were reacted in 50 ml of dry THF to give 1.71 g (50%) of chalcone after purification. 1H NMR (300 MHz, CDCl3): δ 13.07 (s, 1H), 7.95 (d, J=7.8 Hz, 1H), 7.61 (d, J=15.0 Hz, 1H), 7.51-7.42 (m, 2H), 7.02 (d, d, J=0.9, 8.4 Hz, 1H), 6.94 (d, d, d, J=1.2, 8.4, 9.0 Hz, 1H), 6.60 (s, 1H), 2.34 (s, 3H), 2.00 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08715761B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-3b46b34c96ed4eb88b84f8abeac60810 |
| Source note | uspto-grants-2014_05 |