Water → Benzyl 2-(1-aminoethyl)morpholine-4-carboxylate

HRID 2206654Notes

Reaction equation

HRID 2206654 reaction equation
[C:1]([CH:4]1[O:9][CH2:8][CH2:7][N:6]([C:10]([O:12][CH2:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)=[O:11])[CH2:5]1)(=O)[CH3:2].C([O-])(C)=O.[NH4+].[BH3-]C#[N:27].[Na+].O>C1COCC1.CO>[NH2:27][CH:1]([CH:4]1[O:9][CH2:8][CH2:7][N:6]([C:10]([O:12][CH2:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)=[O:11])[CH2:5]1)[CH3:2]

Participants

6

Procedure

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%).

Workup

  1. concentrationThe mixture was concentrated
  2. customto give the crude
  3. extractionthe mixture was extracted by ethyl acetate (60 mL*3), 1N HCl
  4. additionwas added into the combined organic layers
  5. concentrationThe aqueous layer was concentrated
  6. extractionextracted by ethyl acetate (60 mL*3)
  7. washThe organic layer was washed with brine
  8. dry with materialdried over sodium sulfate
  9. concentrationThe mixture was concentrated

Sources & evidence

ORD record
ord-a2677daa602e4c4d8d688d47a9b70c7f
Source dataset
uspto-grants-2016_06
Patent number
US09371331B2

Reaction notes

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