HuagongsheHuagongshe Chemistry Print Report · For research reference only
Citric Acid → (2R)-2-[[(1R)-1-(2-bromophenyl)ethoxy]methyl]oxirane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Citric Acid | HCID 311 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | (R)-1-(2-bromophenyl)ethanol | HCID 2734868 | — |
| Reactant | (R)-(-)-Glycidyl-4-nitrobenzenesulfonate | HCID 14292098 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (2R)-2-[[(1R)-1-(2-bromophenyl)ethoxy]methyl]oxirane | HCID 58981243 | 85.8% |
Reaction Steps
(R)-1-(2-Bromophenyl)ethanol (30.0 g) and (R)-glycidyl nosylate(50.3 g) were dissolved in N,N-dimethylformamide (300 ml), sodium hydride (7.76 g, 60% in oil) was added and the mixture was stirred at room temperature for 2 hr. 10% Aqueous citric acid (600 ml) was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed successively with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane:ethyl acetate=6:1) to give the title compound (32.9 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07285572B2 |
| Source dataset | uspto-grants-2007_10 |
| ORD ID | ord-776297c1bcb04555b20f52f8038e4013 |
| Source note | uspto-grants-2007_10 |