HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → 1,5-Bis-(4-benzyloxy-phenyl)-penta-1,4-dien-3-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Benzaldehyde, 4-(phenylmethoxy)- | HCID 78109 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1,5-Bis-(4-benzyloxy-phenyl)-penta-1,4-dien-3-one | HCID 471475 | — |
Reaction Steps
The title compound was prepared as described in General Method 1 using 42.4 g (0.2 mol) 4-benzyloxybenzaldehyde, 700 mL absolute ethanol (EtOH), 5.8 g (0.1 mol) acetone and 10 mL 10% NaOH. The reaction was refluxed for 2 hours. After cooling the reaction was filtered, and the resultant solid dried. It was used without further purification in the next reaction. 1H NMR (CDCl3) δ 5.11 (s, 4 H), 6.91-7.01 (m, 6 H), 7.34-7.45 (m, 10 H), 7.57 (m, 4 H), 7.69 (d, 2 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05834506 |
| Source dataset | uspto-grants-1998_11 |
| ORD ID | ord-f2f145e690574a919bfda8cca5a19c36 |
| Source note | uspto-grants-1998_11 |