HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 2-(4-tert-butylbenzylidene)-3,4-dihydro-1(2H)-naphthalenone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 1-Tetralone | HCID 10724 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-tert-Butylbenzaldehyde | HCID 70324 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(4-tert-butylbenzylidene)-3,4-dihydro-1(2H)-naphthalenone | HCID 3571213 | — |
Reaction Steps
A mixture of 3,4-dihydro-1(2H)-naphthalenone (4.5 g) and 4-tert-butylbenzaldehyde (5.0 g) was stirred with a solution of 4% potassium hydroxide in methanol (100 ml) for 64 hours at room temperature. The mixture was neutralised with glacial acetic acid, followed by dilution with water (100 ml). The resulting copious white precipitate was filtered off, washed with water and dried in vacuo to give 2-(4-tert-butylbenzylidene)-3,4-dihydro-1(2H)-naphthalenone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05622987 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-392e6da757734f54a4b9ebfe00572a19 |
| Source note | uspto-grants-1997_04 |