Ethylamine → 1-Benzyl-3-ethylaminomethyl-3-hydroxypyrrolidine
Reaction equation
[CH2:1]([N:8]1[CH2:14][CH2:13][C:10]2([O:12][CH2:11]2)[CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH2:15]([NH2:17])[CH3:16]>>[CH2:1]([N:8]1[CH2:14][CH2:13][C:10]([CH2:11][NH:17][CH2:15][CH3:16])([OH:12])[CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Participants
3
Procedure
10.2 g (53.9 mmol) of 5-benzyl-5-aza-1-oxaspiro-[2,4]heptane are added dropwise to 60 ml of aqueous ethylamine solution (50%) and the mixture is stirred overnight at room temperature. The batch is then concentrated and the residue is distilled.
Workup
- concentrationThe batch is then concentrated
- distillationthe residue is distilled
Sources & evidence
- ORD record
- ord-5ad06185ef514c8b814da9835bd1dce6
- Source dataset
- uspto-grants-1995_09
- Patent number
- US05453422
Reaction notes
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