HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → HCID 21510503, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Salicylaldehyde | HCID 6998 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | p-Chlorophenacyl bromide | HCID 68303 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21510503 | HCID 21510503 | — |
Reaction Steps
To a solution of 15.3 g. (0.125 mol.) of salicylaldehyde in 100 ml. of acetone was added 7.0 g. (0.125 mol.) of potassium hydroxide dissolved in a minimum amount of water. α-Bromo-p-chloroacetophenone (29.16 g., 0.125 mol.) was added dropwise with stirring and cooling (ice bath). After addition, the reaction mixture was stirred at 25° for 12 hours. The precipitate was collected by filtration, washed with water and combined with the residue remaining after concentration of the filtrate to give 2-(4'-chlorobenzoyl)-3-hydroxycoumaran which was immediately dehydrated in the presence of p-toluenesulfonic acid to yield 2-(4'-chlorobenzoyl)benzofuran.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03975537 |
| Source dataset | uspto-grants-1976_08 |
| ORD ID | ord-0bf8ae4dc77b49cda667974a44fd62a8 |
| Source note | uspto-grants-1976_08 |