HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → [1-(3-Bromophenyl)-2-(4-morpholinyl)ethyl]methylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 1-(3-Bromophenyl)-2-(4-morpholinyl)ethanone | HCID 20823746 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [1-(3-Bromophenyl)-2-(4-morpholinyl)ethyl]methylamine | HCID 57501274 | 100.3% |
Reaction Steps
To a solution of 1-(3-bromophenyl)-2-(4-morpholinyl)ethanone (7.8 g, 27.0 mmol) in THF (50 mL) was added methylamine (100 mL, 200 mmol, 2M solution in THF). After stirring for 15 min at room temperature, sodium cyanoborohydride (3.40 g, 54 mmol) was added followed by acetic acid (2 mL). The resultant mixture was stirred at RT for 5 days. The mixture was concentrated under reduced pressure. The residue was dissolved in ethyl acetate (200 mL) and washed with 5% NaHCO3 (200 mL) and brine (200 mL). The organic layer was dried (MgSO4) and concentrated to give [1-(3-bromophenyl)-2-(4-morpholinyl)ethyl]methylamine as yellow oil (8.10 g, 100%) which solidified after standing at room temperature. MS (ESI): 299.6 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07432258B2 |
| Source dataset | uspto-grants-2008_10 |
| ORD ID | ord-af173e9b66af485e88b2a2aae1d99e84 |
| Source note | uspto-grants-2008_10 |