HuagongsheHuagongshe Chemistry Print Report · For research reference only
Morpholine → 4-Morpholinebutanamide, N-methoxy-N-methyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-chloro-N-methoxy-N-methylbutyramide | HCID 11252200 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-Morpholinebutanamide, N-methoxy-N-methyl- | HCID 11390303 | 44.2% |
Reaction Conditions
| Temperature | 105 °C |
|---|
Reaction Steps
To a solution of the product from Step 1 (3.01 g, 18.1 mmol) in MeCN (40 mL), was added K2CO3 (10 g, 72.4 mmol) and morpholine (1.58 mL, 18.1 mmol). This mixture was then heated to 105° C. in a sealed tube for overnight. The reaction mixture then diluted with MeCN (50 mL), then filtered and concentrated. Residue was taken up in Et2O (100 mL), washed with brine, dried over Na2SO4, filtered and concentrated to afford the title compound as a colorless oil (1.73 g, 44%), which was used directly to next step without further purification. MS (ES+) m/e 217 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07547779B2 |
| Source dataset | uspto-grants-2009_06 |
| ORD ID | ord-f5949b362bd04e0aa6ab015cd81d25e2 |
| Source note | uspto-grants-2009_06 |