HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → 2-Benzylidene-3,4-dihydronaphthalen-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | 1-Tetralone | HCID 10724 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Benzylidene-3,4-dihydronaphthalen-1-one | HCID 111179 | — |
Reaction Steps
A 250 mL flask was charged with tetralone (4 g, 27.4 mmol) and benzaldehyde (3.88 g, 36.6 mmol). This was dissolved in warm tetrahydrofuran (15 mL), and to this yellow solution was slowly added a 4 wt % solution of KOH in methanol (125 mL). The reaction was stirred for 4 days at room temperature. The solvent was then removed under reduced pressure, and it was poured into 150 mL of water and extracted with methylene chloride. The organic extract was dried over magnesium sulfate and filtered, and the solvent was removed at reduced pressure to afford 4.1 g (64%) as white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09040175B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-bf428d9552f342caab4e5241e9dfdf60 |
| Source note | uspto-grants-2015_05 |