HuagongsheHuagongshe Chemistry Print Report · For research reference only
Morpholine → HCID 86716006, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Trimethylsilyl cyanide | HCID 82115 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Pyrimidine-5-carboxaldehyde | HCID 2761034 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 86716006 | HCID 86716006 | 66.1% |
Reaction Steps
To a mixture of pyrimidine-5-carbaldehyde (2 g, 18.52 mmol) and TMSCN (3.67 g, 37.0 mmol) in HOAc (50 mL) was added morpholine (2.42 g, 27.8 mmol) at room temperature and NaOAc (3.34 g, 40.7 mmol) was followed. The resulting mixture was stirred at room temperature overnight. Saturated aqueous Na2CO3 solution was added to quench the reaction mixture, the pH was adjusted to about 7 and extracted with EtOAc (3×100 mL). The combined organic layer was washed with brine, dried over Na2SO4 and concentrated to give crude 2-morpholino-2-(pyrimidin-5-yl)acetonitrile (2.5 g, yield: 66%). 1H NMR (CDCl3 400 MHz): δ9.25 (s, 1H), 8.92 (d, J=10.0 Hz, 2H), 4.87 (s, 1H), 3.79-3.70 (m, 4H), 2.67-2.56 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09108938B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-7e63bfbe78cb4850834674e24f83883f |
| Source note | uspto-grants-2015_08 |