HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Nitrophenol → (R)-2,2-dimethyl-4-((3-nitrophenoxy)methyl)-1,3-dioxolane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Nitrophenol | HCID 11137 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (R)-(+)-4-(Chloromethyl)-2,2-dimethyl-1,3-dioxolane | HCID 2734443 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (R)-2,2-dimethyl-4-((3-nitrophenoxy)methyl)-1,3-dioxolane | HCID 58552880 | 52% |
Reaction Conditions
| Temperature | 160 °C |
|---|
Reaction Steps
3-Nitrophenol (2.0 g, 14.37 mmol) was taken up in 20 mL of anhydrous DMF along with anhydrous potassium carbonate (4.96 g, 35.93 mmol) and (R)-4-(chloromethyl)-2,2-dimethyl-1,3-dioxolane (2.55 mL, 18.68 mmol). The resulting reaction mixture was heated in the microwave reactor, with stirring, at 160° C. for 4 h. The crude reaction mixture was rinsed with water, filtered and extracted with dichloromethane (3×15 mL). The combined organic layers were dried (Na2SO4) and concentrated under reduced pressure. The resulting residue was purified by chromatography using ethyl acetate: pentane to obtain the desired product as an amber-colored oil (52%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08685970B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-a6b43f4bb01547fc9afadc59964bb7fd |
| Source note | uspto-grants-2014_04 |