HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4-(4-Morpholinylcarbonyl)phenyl trifluoromethanesulphonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | (4-Hydroxyphenyl)(morpholino)methanone | HCID 7586556 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(4-Morpholinylcarbonyl)phenyl trifluoromethanesulphonate | HCID 17982865 | — |
Reaction Conditions
| Temperature | -10 °C |
|---|
Reaction Steps
1.23 ml (7.24 mmol) of trifluoromethanesulphonic anhydride are slowly added dropwise to a solution, cooled to −10° C., of 1.0 g (4.83 mmol) of 4-(4-morpholinylcarbonyl)phenol and 2.02 ml (14.48 mmol) of triethylamine in 20 ml of dichloromethane. The mixture is stirred at −10° C. for 30 min and then at 0° C. for 30 min. It is washed successively with 10% strength sodium bicarbonate solution, water and saturated sodium chloride solution, dried over sodium sulphate and concentrated in vacuo, and the residue is dried under high vacuum. 1.71 g (94.6% of theory) of the title compound are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07977485B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-606698efdf6a4407bb74b88ebb47cbb7 |
| Source note | uspto-grants-2011_07 |