HuagongsheHuagongshe Chemistry Print Report · For research reference only
Morpholine → 4-(1-(4-Nitrophenyl)ethyl)morpholine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(1-Bromoethyl)-4-nitrobenzene | HCID 11020679 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(1-(4-Nitrophenyl)ethyl)morpholine | HCID 13398803 | 95.5% |
Reaction Steps
A mixture of 1-(1-bromo-ethyl)-4-nitro-benzene (1.24 g, 5.43 mmol), potassium carbonate (2.25 g, 16.3 mmol) and morpholine (1.2 mL, 13.6 mmol) in DMF (10 mL) was stirred at room temperature for 16 h, then evaporated. The residue was suspended in ethyl acetate, washed with water and brine, dried (sodium sulfate) and evaporated to provide 4-[1-(4-nitro-phenyl)-ethyl]-morpholine (1.225 g, 95% yield) as a yellow oil. 1H-NMR (DMSO-d6, 500 MHz) 8.19 (d, 2H), 7.16 (d, 2H), 3.56 (m, 5H), 2.41 (m, 2H), 2.26 (m, 2H), 1.29 (d, 3H) ppm; MS (FIA) 237.2 (M+H); HPLC (Method A) 2.248 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07902239B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-f4aa02a0c348409f8fd080535183ed74 |
| Source note | uspto-grants-2011_03 |