HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol, 1-ethoxy-2,2,2-trifluoro- → Trifluoroacetaldehyde {2-chloro-4-methyl-5-(2,2,2-trifluoroethylthio)phenyl}hydrazone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol, 1-ethoxy-2,2,2-trifluoro- | HCID 9897 | — |
| Reactant | 2-Chloro-4-methyl-5-(2,2,2-trifluoroethylthio)phenylhydrazine | HCID 66841936 | — |
| Catalyst | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Trifluoroacetaldehyde {2-chloro-4-methyl-5-(2,2,2-trifluoroethylthio)phenyl}hydrazone | HCID 86628937 | 67.8% |
Reaction Steps
A mixture of 4.1 g of 2-chloro-4-methyl-5-(2,2,2-trifluoroethylthio)phenylhydrazine, 2.3 g of trifluoroacetaldehyde ethyl hemiacetal, 0.1 g of p-toluenesulfonic acid monohydrate and 50 ml of ethanol was refluxed with heating for 6 hours. The obtained reaction mixture was concentrated under reduced pressure, water was added, and the mixture was extracted with toluene. The organic layer was washed with water and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure to obtain 3.6 g of trifluoroacetaldehyde {2-chloro-4-methyl-5-(2,2,2-trifluoroethylthio)phenyl}hydrazone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07872036B2 |
| Source dataset | uspto-grants-2011_01 |
| ORD ID | ord-6cb27ba9bd1347ed8de689626fd87816 |
| Source note | uspto-grants-2011_01 |