HuagongsheHuagongshe Chemistry Print Report · For research reference only
alpha-Hydroxyacetophenone → Cinnamoylbenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | alpha-Hydroxyacetophenone | HCID 68490 | — |
| Reactant | 1,3-Thiazole-2-carbaldehyde | HCID 2734903 | — |
| Reactant | HCID 178418582 | HCID 178418582 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Cinnamoylbenzene | HCID 7189 | 27% |
Reaction Steps
2.29 g (16.8 mmol) of 2-hydroxyacetophenone, 1.8 g of thiazole-2-carbaldehyde (15.9 mmol), and 10 ml of 25% wt NaOCH3 were reacted in 50 ml of dry THF to give 0.254 g (27%) of chalcone after purification. 1H NMR (300 MHz, CDCl3): δ 12.62 (s, 1H), 8.08-7.94 (m, 4H), 7.57-7.51 (m, 2H), 7.06 (d, d, J=1.2, 8.4 Hz, 1H), 6.98 (d, d, d, J=1.2, 7.2, 8.1 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08449936B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-9fcf0ea61aee4fd2af2d721ecc79470b |
| Source note | uspto-grants-2013_05 |