HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Tetralone → ST50113612
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Tetralone | HCID 10724 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-Bromobenzaldehyde | HCID 70741 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | ST50113612 | HCID 1549209 | 96% |
Reaction Steps
A 250 mL flask was charged with tetralone (3.22 g, 22 mmol) and 4-bromobenzaldehyde (5.3 g, 28.6 mmol). This was dissolved in warm tetrahydrofuran (12 mL), and to this yellow solution was slowly added a 4 wt % solution of KOH in methanol (100 mL). The reaction was stirred for 4 days at room temperature. The mixture was concentrated and reduced to approx 10% vol. The residue was filtered and washed with MTBE (3*50 mL), dried, to afford a light yellow powder (6.61 g, 96%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09040175B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-d7cc6d1dbe2549e3ba7b865c93fc5fdd |
| Source note | uspto-grants-2015_05 |