HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → 3-(4-Hydroxyphenyl)-1-phenylprop-2-en-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4'-Hydroxyacetophenone | HCID 7469 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Product | 3-(4-Hydroxyphenyl)-1-phenylprop-2-en-1-one | HCID 89340 | 50% |
Reaction Steps
The photo-reactive group of the side chain was synthesized as follows. First, 10.2 g (0.075 mol) of 4-hydroxyacetophenone was dissolved into 0.7 w/v % aqueous solution of NaOH. Benzaldehyde (8 g (0.075 mol)) then was added and the resulting solution was stirred for 8 hours at a room temperature. Then, the solution was neutralized with 5N HCl to yield 4-hydroxychalcone at 50% yield as follows.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06858269B2 |
| Source dataset | uspto-grants-2005_02 |
| ORD ID | ord-4ebde6e3e5484ef4a7fc46cc20cef663 |
| Source note | uspto-grants-2005_02 |