HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetyl chloride → Isopropyl 2-(morpholinoamino)-4-oxo-4,5-dihydrofuran-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | N-Aminomorpholine | HCID 20315 | — |
| Reactant | Diisopropyl malonate | HCID 83223 | — |
| Reactant | Isopropyl 2-isopropoxy-4-oxo-4,5-dihydrofuran-3-carboxylate | HCID 51050080 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Isopropyl 2-(morpholinoamino)-4-oxo-4,5-dihydrofuran-3-carboxylate | HCID 86708411 | — |
Reaction Steps
To a solution of isopropyl 2-isopropoxy-4-oxo-4,5-dihydrofuran-3-carboxylate (12.2 g, 53.6 mmol), which similarly prepared according to the procedure described in the Example 74, Third step using diisopropyl malonate and chloroacetyl chloride, in ethanol (45 mL), 4-aminomorpholine (5.7 mL, 59.2 mmol) was added at ambient temperature. The mixture was stirred for 18 h. The solvent was removed under reduced pressure, and the crude product was suspended in methyl tert-butyl ether, then the precipitate was collected by filtration, washed with methyl tert-butyl ether and hexane then dried to afford isopropyl 2-(morpholinoamino)-4-oxo-4,5-dihydrofuran-3-carboxylate as solid (11.2 g, y. 75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08742113B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-9401091bbd5f4cd7bb2ee7a7c88ee7d2 |
| Source note | uspto-grants-2014_06 |