HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2,3-Dimethyl-4-nitrophenyl trifluoromethanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Trifluoromethanesulfonate | HCID 2758875 | — |
| Reactant | 2,3-Dimethyl-4-nitrophenol | HCID 13331245 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,3-Dimethyl-4-nitrophenyl trifluoromethanesulfonate | HCID 22933396 | 99.3% |
Reaction Steps
Anhydrous trifluoromethanesulfonate (3.17 ml, 18.8 mmol) and triethylamine (2.75 ml, 19.7 mmol) were added dropwise to a solution of 2,3-dimethyl-4-nitrophenol (3.0 g, 17.9 mmol) in methylene chloride (60 ml) at 0° C. and stirred at room temperature for 1 hour. Then, the reaction solution was poured into water and extracted with chloroform. The organic layer was dried over magnesium sulfate and distilled to remove the solvent, and the resulting residue was purified by a silica gel column chromatography (eluent: hexane/ethyl acetate) to obtain 2,3-dimethyl-4-nitrophenyl trifluoromethanesulfonate (5.32 g, 99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07199147B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-d409822078ca4533832eb0b390a64316 |
| Source note | uspto-grants-2007_04 |