HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclohexanone → 2,6-Bis-(4-hexyloxy-benzylidene)-cyclohexanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclohexanone | HCID 7967 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | p-(Hexyloxy)benzaldehyde | HCID 79816 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,6-Bis-(4-hexyloxy-benzylidene)-cyclohexanone | HCID 69497980 | — |
Reaction Steps
Cyclohexanone (2.6 ml, 0.025 mol) was dissolved in ethanol (5 ml), and was added to sodium hydroxide (0.38 g, 0.01 mol) dissolved in water (6 ml) and ethanol (2 ml) and was left to stir for 20 min. 4-Hexyloxybenzaldehyde (10 ml, 0.048 mol), dissolved in ethanol (40 ml), was added and the mixture was stirred at room temperature for 16 h. A yellow crystalline solid was isolated by vacuum filtration and was washed with cold ethanol and dried in a vacuum oven. Yield=4.32 g, 36%. 1H NMR and 13C NMR showed expected signals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06939479B2 |
| Source dataset | uspto-grants-2005_09 |
| ORD ID | ord-affe587f4e1d4c599e66c79b12e2f716 |
| Source note | uspto-grants-2005_09 |