HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Chloro-4-morpholinoaniline → N-(3-chloro-4-morpholinophenyl)-3-oxobutanamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Chloro-4-morpholinoaniline | HCID 108661 | — |
| Reactant | But-1-ene-1,3-dione | HCID 12642904 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-(3-chloro-4-morpholinophenyl)-3-oxobutanamide | HCID 90022603 | 91% |
Reaction Steps
To a solution of 3-chloro-4-morpholinoaniline (2.05 g, 9.64 mmol) in EtOAc (30 mL) was added acetyl ketene (1.62 g, 19.3 mmol) with stirring and the mixture was stirred at 80° C. overnight. The mixture was cooled to rt and concentrated in vacuo. The residue was purified by a silica gel column chromatography (PE/EtOAc (V/V)=3:1) to give the title compound as a pale yellow solid (2.59 g, 91%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09434695B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-37bf6db4682043d784aacf127e737472 |
| Source note | uspto-grants-2016_09 |