HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Nitrate → 2-[(2-Chloro-4-fluoro-5-nitrophenyl)methyl]-4,4-dimethyl-3-isoxazolidinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Nitrate | HCID 24434 | — |
| Reactant | 2-[(2-Chloro-4-fluorophenyl)methyl]-4,4-dimethyl-1,2-oxazolidin-3-one | HCID 13192573 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | 2-[(2-Chloro-4-fluoro-5-nitrophenyl)methyl]-4,4-dimethyl-3-isoxazolidinone | HCID 20032374 | 50.8% |
Reaction Steps
By the method of Example 3, Step A, 20 g (0.078 mole) of 2-[(2-chloro-4-fluorophenyl)methyl]-4,4-dimethyl-3-isoxazolidinone, 7.8 g (0.78 mole) of potassium nitrate, and 100 ml of concentrated sulfuric acid were reacted, yielding 12 g of 2-[(2-chloro-4-fluoro-5-nitrophenyl)methyl]-4,4-dimethyl-3-isoxazolidinone as a light yellow solid. Passage through a column of silica gel was omitted since the product was crystalline. Purification was accomplished by recrystallization from ethyl acetate/hexane. This reaction was repeated, and the products were combined.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04846882 |
| Source dataset | uspto-grants-1989_07 |
| ORD ID | ord-f6ac26398fa44f38b55a50718fbb3436 |
| Source note | uspto-grants-1989_07 |