Reaction equation
[NH2:1][CH:2]1[CH2:6][C:5]2([CH2:11][CH2:10][CH:9]([C:12]([CH3:15])([CH3:14])[CH3:13])[CH2:8][CH2:7]2)[O:4][CH2:3]1.[CH3:16][CH2:17][CH2:18][C:19](=O)[CH2:20][CH2:21][CH3:22].C([BH3-])#N.[Na+].[OH-].[Na+]>CO.[Cl-].[Zn+2].[Cl-].C1(C)C=CC=CC=1>[CH3:16][CH2:17][CH2:18][CH:19]([NH:1][CH:2]1[CH2:6][C:5]2([CH2:7][CH2:8][CH:9]([C:12]([CH3:15])([CH3:14])[CH3:13])[CH2:10][CH2:11]2)[O:4][CH2:3]1)[CH2:20][CH2:21][CH3:22]Participants
8
Reactant 4
Product 1
Reagents, catalysts & solvents 3
Procedure
To 3-amino-8-t-butyl-1-oxaspiro(4,5)-decane (1.12 g, 5 mmol) and heptane-4-one (0.6 g, 5.25 mmol) in dry methanol (20 ml) was added zinc chloride (0.41 g, 3 mmol). The mixture was stirred at room temperature for 5 minutes and sodium cyanoborohydride 0.38 g, 6 mmol) was added and the resulting heterogeneous mixture was stirred at room temperature overnight. The solvent was then stripped off in vacuo, toluene (50 ml) and 2N NaOH (50 ml) was added. The aqueous phase was extracted twice with toluene (2×50 ml) and the combined organic layers were dried (MgSO4) and concentrated in vacuo. The resulting oil was purified by flash chromatography to give a pale yellow oil (1.12 g). nD22 :1.4726.
Workup
- stirringthe resulting heterogeneous mixture was stirred at room temperature overnight
- additionwas added
- extractionThe aqueous phase was extracted twice with toluene (2×50 ml)
- dry with materialthe combined organic layers were dried (MgSO4)
- concentrationconcentrated in vacuo
- customThe resulting oil was purified by flash chromatography
Sources & evidence
- ORD record
- ord-acfcef81c8034919b2eee27bae2f0bf5
- Source dataset
- uspto-grants-1997_01
- Patent number
- US05591741
Linked notes
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