HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoromethanesulfonic anhydride → (2-Cyano-5-methoxyphenyl)trifluoromethanesulphonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | 2-Hydroxy-4-methoxybenzonitrile | HCID 11423680 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | (2-Cyano-5-methoxyphenyl)trifluoromethanesulphonate | HCID 19771853 | 81.1% |
Reaction Steps
Trifluoromethanesulphonic anhydride (2.06 g) was added dropwise to a solution of 2-cyano-5-methoxyphenol (1.0 g) in dry pyridine (20 ml) at 0° C. under an atmosphere of argon. Volatile material was removed by evaporation and the residue was dissolved in ethyl acetate (30 ml). The solution was washed with water (60 ml) and saturated sodium chloride solution (30 ml) and dried (MgSO4). The solvent was removed by evaporation and the residue purified by flash chromatography, eluting with ethyl acetate/hexane (1:3 v/v), to give (2-cyano-5-methoxyphenyl)trifluoromethanesulphonate (1.53 g) as an oil; NMR (CDCl3): 3.9(s,3H), 6.95(d,1H), 7.0(d,1H), 7.7(d,1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05130318 |
| Source dataset | uspto-grants-1992_07 |
| ORD ID | ord-d2d74b3b03554563a9e3a6dc878eec83 |
| Source note | uspto-grants-1992_07 |