HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclohexyl methyl ketone → 3-(4-Benzyloxy-phenyl)-1-cyclohexyl-prop-2-en-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclohexyl methyl ketone | HCID 13207 | — |
| Reactant | Benzaldehyde, 4-(phenylmethoxy)- | HCID 78109 | — |
| Reactant | Barium hydroxide | HCID 6093286 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(4-Benzyloxy-phenyl)-1-cyclohexyl-prop-2-en-1-one | HCID 471477 | — |
Reaction Steps
The title compound was prepared as described in General Method 2 using 17.40 g (138 mmol) of cyclohexyl methyl ketone, 29.26 g (138 mmol) of 4-benzyloxybenzaldehyde, 3.17 g of barium hydroxide (anhydrous), and 300 mL of 95% EtOH. The reaction was heated at reflux for eight hours. The crude product was recrystallized from EtOAc. The 25.85 g of product, contaminated with some 4-benzyloxybenzaldehyde, was taken on without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06046355 |
| Source dataset | uspto-grants-2000_04 |
| ORD ID | ord-62c3f2b409b7437bb8b2f41c43f136a0 |
| Source note | uspto-grants-2000_04 |