HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → HCID 70637539, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Chloro-4-methylbenzaldehyde | HCID 13553331 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 70637539 | HCID 70637539 | — |
Reaction Steps
The starting material, 1,5-bis(3-chloro-p-tolyl)-1,4-pentadien-3-one is prepared by the reaction of two moles of 3-chloro-p-tolualdehyde [Wahl, Ann. Chim. [11] 5 (1936), pp. 5, 39] and one mole of acetone in ethanol solution in the presence of sodium hydroxide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | USRE029358 |
| Source dataset | uspto-grants-1977_08 |
| ORD ID | ord-c36598c1ebda4aa8af4efa80b86eef47 |
| Source note | uspto-grants-1977_08 |