HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 54332237, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 2,4-Dichlorobenzaldehyde | HCID 13404 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 14348392 | HCID 14348392 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 54332237 | HCID 54332237 | 97.6% |
Reaction Steps
5 pellets of solid sodium hydroxide are added at room temperature to a mixture of 41.7 g (0.26 mol) of 1-acetyl-1-propylmercapto-cyclopropane, 46 g (0.26 mol) of 2,4-dichlorobenzaldehyde, 130 ml of ethanol and 30 ml of dichloromethane. The mixture is stirred for a further 14 hours at room temperature. 50 ml of water are added, and the oil phase is separated off and taken up in dichloromethane. The organic phase is washed using water, dried over sodium sulphate and concentrated by stripping off the solvent under reduced pressure. In this manner, 80 g (97% of theory) of 2,4-dichlorophenyl-ethenyl 1-propylmercaptocyclopropyl ketone (cis-trans isomers) are obtained in the form of an oily product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04983208 |
| Source dataset | uspto-grants-1991_01 |
| ORD ID | ord-0add9d15b5874464bc4abdeae53eef47 |
| Source note | uspto-grants-1991_01 |