HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → HCID 236807, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | P-Chloroacetophenone | HCID 7467 | — |
| Product | HCID 236807 | HCID 236807 | 91.9% |
Reaction Steps
To a solution of benzaldehyde (2 g) in EtOH (40 ml) 3 M NaOH solution (3 eq) and 4-chloroacetophenone (2.91 g) were added. The resulting mixture was stirred at rt for 2 h forming a yellow precipitate. The solid was separated by suction filtration and washed with water. The crude was purified by recrystallisation from methanol to give 1-(4-chlorophenyl)-3-phenylprop-2-en-1-one (4.2 g) as pale yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08912186B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-a2a4c9dee50c42a389ceed021bb7f4c2 |
| Source note | uspto-grants-2014_12 |