HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Methyl-2-butanone → 2-Methyl-2-(trifluoromethylthio)butan-3-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Methyl-2-butanone | HCID 11251 | — |
| Reactant | Methanesulfenyl chloride, trifluoro- | HCID 67900 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Methyl-2-(trifluoromethylthio)butan-3-one | HCID 13117300 | 80.7% |
Reaction Steps
334 g of methyl isopropyl ketone in 1.2 liters of methylene chloride were initially introduced into a narrow stirred vessel equipped with a condenser. 220 g of trifluoromethane-sulphenyl chloride were introduced, at room temperature in the course of 4 hours, through an inlet tube extending to the bottom of the vessel. The reaction mixture was allowed to stand overnight. It was then distilled. 242 g (80.7% of theory) of crude 3-methyl-3-trifluoromethylthio-butan-2-one were obtained and purified by fractional distillation: boiling point: 60° C./50 mbar and refractive index nD20 =1.4030. ##STR12##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04629732 |
| Source dataset | uspto-grants-1986_12 |
| ORD ID | ord-8e3b9fac0f7a425a9240cd8cff7bca01 |
| Source note | uspto-grants-1986_12 |