HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → HCID 131733310, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 117830854 | HCID 117830854 | — |
| Reactant | HCID 117831294 | HCID 117831294 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | HCID 131733310 | HCID 131733310 | — |
Reaction Steps
To a suspension of 1 g of NaH (60%) (25.08 mmol) in 30 mL of MTBE there are added, dropwise, a solution of 5 g of tert-butyl 3-morpholino-3-oxopropanoate (21.81 mmol) in 20 mL of anhydrous MTBE. This suspension is stirred at ambient temperature for 1 hour and then the compound obtained in Step A is added in the form of a powder. The batch is stirred at 60° C. for 30 hours. 100 mL of saturated aqueous ammonium chloride solution are added. The resulting solution is extracted with dichloromethane. The organic phase is then dried over MgSO4, filtered and concentrated to dryness. After purification by chromatography over silica gel (dichloromethane/MeOH gradient), the expected product is obtained in the form of an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09115159B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-a7ac8f5fae1c473dab054c960a386142 |
| Source note | uspto-grants-2015_08 |