Ethanolamine → trans-1-Benzyl-4-hydroxy-3-(2-hydroxyethylamino)pyrrolidine
Reaction equation
[CH2:1]([N:8]1[CH2:13][CH:12]2[CH:10]([O:11]2)[CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[NH2:14][CH2:15][CH2:16][OH:17]>O>[CH2:1]([N:8]1[CH2:9][C@@H:10]([OH:11])[C@H:12]([NH:14][CH2:15][CH2:16][OH:17])[CH2:13]1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
40 g (0.22 mol) of 3-benzyl-6-oxa-3-azabicyclo[3.1.0]hexane are heated under reflux with 42 g (0.68 mol) of 2-aminoethanol in 450 ml of water overnight. The solution is extracted once with tert.-butyl methyl ether and the aqueous phase is concentrated. The residue is distilled.
Workup
- extractionThe solution is extracted once with tert.-butyl methyl ether
- concentrationthe aqueous phase is concentrated
- distillationThe residue is distilled
Sources & evidence
- ORD record
- ord-5e0b272a0f31494d8037c87ba38669d2
- Source dataset
- uspto-grants-1995_05
- Patent number
- US05416096
Reaction notes
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