HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-Morpholin-4-ylphenyl trifluoromethanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | 3-Morpholinophenol | HCID 141343 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Morpholin-4-ylphenyl trifluoromethanesulfonate | HCID 17982677 | — |
Reaction Conditions
| Temperature | -10 °C |
|---|
Reaction Steps
2.18 ml (12.9 mmol) of trifluoromethanesulphonic anhydride are slowly added dropwise to a solution, cooled to −10° C., of 1.54 g (8.6 mmol) of 3-(4-morpholinyl)-phenol and 3.59 ml (25.8 mmol) of triethylamine in 10 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. 2.41 g (90.1% 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-06c6d00ea438451a84039a7197f688a4 |
| Source note | uspto-grants-2011_07 |