HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Benzyl 2-(1-aminoethyl)morpholine-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | Phenylmethyl 2-acetyl-4-morpholinecarboxylate | HCID 18354411 | — |
| Solvent | MeOH tetrahydrofuran | HCID 21899815 | — |
| Product | Benzyl 2-(1-aminoethyl)morpholine-4-carboxylate | HCID 18354340 | 40% |
Reaction Steps
To a solution of benzyl 2-acetylmorpholine-4-carboxylate (5.0 g, 19 mmol) in THF/MeOH (1/5, 100 mL) were added AcONH4 (14.6 g, 190 mmol) and NaBH3CN (11.8 g, 190 mmol). The mixture was stirred at room temperature for 50 hr. The mixture was concentrated to give the crude. Water (20 mL) was added and the mixture was extracted by ethyl acetate (60 mL*3), 1N HCl, was added into the combined organic layers. The aqueous layer was concentrated, brought to above pH>8 with 2N NaOH and extracted by ethyl acetate (60 mL*3). The organic layer was washed with brine, dried over sodium sulfate. The mixture was concentrated to give benzyl 2-(1-aminoethyl)morpholine-4-carboxylate (2.0 g, 40%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09371331B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-a2677daa602e4c4d8d688d47a9b70c7f |
| Source note | uspto-grants-2016_06 |