HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiomorpholine → 4-(2,6-Difluoro-4-nitrophenyl)thiomorpholine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiomorpholine | HCID 67164 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1,2,3-Trifluoro-5-nitrobenzene | HCID 2782793 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-(2,6-Difluoro-4-nitrophenyl)thiomorpholine | HCID 12096592 | — |
Reaction Steps
A solution of 3,4,5-trifluoronitrobenzene (5.00 g, 28.24 mmol) in acetonitrile (60 mL) is cooled to 0° C. and treated with N,N-diisopropylethylamine (7.38 mL, 42.35 mmol) followed by thiomorpholine (2.98 mL, 29.65 mmol). The ice bath is removed and the reaction mixture stirred at room temperature under nitrogen for approximately 24 h, during which additional thiomorpholine (0.1 eq) is added. The solvent is removed under reduced pressure, and the residue is diluted with ethyl acetate, washed with 1N hydrochloric acid (until the washings are acidic), saturated aqueous sodium bicarbonate and saline, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to give the title compound, mp 104-105° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06919329B2 |
| Source dataset | uspto-grants-2005_07 |
| ORD ID | ord-49a6800b262043928cdb8445e17fd0f0 |
| Source note | uspto-grants-2005_07 |