HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroxylamine HCl → N-[2,2,2-Trifluoro-1-(2-methylphenyl)ethylidene]hydroxylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroxylamine HCl | HCID 21645 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 2,2,2-Trifluoro-1-(2-methylphenyl)ethan-1-one | HCID 13238647 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-[2,2,2-Trifluoro-1-(2-methylphenyl)ethylidene]hydroxylamine | HCID 71329090 | 66.4% |
Reaction Steps
3.7 g (0.020 mol) of 2,2,2-trifluoro-1-(2-methylphenyl)-ethanone are dissolved in 20 ml of ethanol at 80° C. To the solution are added dropwise 1.4 g (0.020 mol) of hydroxylammonium chloride and 2.7 g (0.033 mol) of sodium acetate dissolved in 10 ml of water. The reaction mixture is refluxed for 5 hours, poured into ice water, and extracted with ethyl acetate. The organic phase is washed with water and brine, dried over MgSO4, and concentrated, yielding 2.7 g of 2,2,2-trifluoro-1-(2-methylphenyl)-ethanone oxime as a white solid. The crude product is used in the next reaction step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06512020B1 |
| Source dataset | uspto-grants-2003_01 |
| ORD ID | ord-cc9e921166f84df498f56db3a520fac5 |
| Source note | uspto-grants-2003_01 |