HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → 3-Bromo-4,4-dimethyloxazolidin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 4,4-Dimethyl-1,3-oxazolidin-2-one | HCID 141315 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 3-Bromo-4,4-dimethyloxazolidin-2-one | HCID 94595 | — |
Reaction Steps
12.3 g (0.11 mol) 4,4-dimethyl-2-oxazolidinone was dissolved in 180 ml of 1 M sodium hydroxide and the resulting solution was cooled to 0°. 19.2 g (0.012 mol) bromine was added dropwise with stirring over 0.25 hr and the reaction mixture was stirred at 0° for an additional 0.75 hr. The N-bromamine separated from the reaction mixture as an orange colored solid. The solid was isolated by filtration and thoroughly washed with cold water. Trituration of this material in petroleum ether (30°-60°) gave 16.2 g (0.084 mol), 76%, 3-bromo-4,4-dimethyl-2-oxazolidinone (NBDMO), mp 118°-120°; uv (H2O) λmax 274 nm, ε= 201 M-1 cm-1 ; ir (KBr): 2985, 1725, 1370, 1290, 1200, 1165, 1040 and 740 cm-1 ; pmr (CDCl3) δ 4.27 (s, 2H) and 1.33 (s, 6H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04009178 |
| Source dataset | uspto-grants-1977_02 |
| ORD ID | ord-03d3fe2baf1b4665aeaf91f3bce9da99 |
| Source note | uspto-grants-1977_02 |