HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Propanone, 1-(acetyloxy)-3-chloro- → Diethyl [(2,3,4-trifluoroanilino)(3-acetoxy-2-oxopropylthio)methylene]malonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Propanone, 1-(acetyloxy)-3-chloro- | HCID 38413 | — |
| Reactant | HCID 178472269 | HCID 178472269 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Diethyl [(2,3,4-trifluoroanilino)(3-acetoxy-2-oxopropylthio)methylene]malonate | HCID 14390992 | 91% |
Reaction Steps
Diethyl [(2,3,4-trifluoroanilino)(mercapto)methylene]malonate sodium salt (5.3 g) was dissolved in N,N-dimethylformamide (70 ml) and thereo 1-acetoxy-3-chloroacetone (2.2 g) was added and the mixture was stirred at room temperature for 30 minutes. The reaction mixture was filtered to remove insoluble materials. After the filtrate was evaporated to dryness under reduced pressure, water was added to the residue and the mixture was extracted with chloroform. The extract was washed with a NaCl solution and dried over anhydrous magnesium sulfate, followed by distilling off the solvent under reduced pressure to give the title compound (6.0 g) as pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04808584 |
| Source dataset | uspto-grants-1989_02 |
| ORD ID | ord-79e335fdd4f24cf792a38d53a3cdc60c |
| Source note | uspto-grants-1989_02 |