Acetic Acid → (S)-methyl 2-(bis(4-methoxybenzyl)amino)-2-phenylacetate
Reaction equation
[CH3:1][O:2][C:3]1[CH:21]=[CH:20][C:6]([CH2:7][NH:8][C@@H:9]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[C:10]([O:12][CH3:13])=[O:11])=[CH:5][CH:4]=1.[CH3:22][O:23][C:24]1[CH:31]=[CH:30][C:27]([CH:28]=O)=[CH:26][CH:25]=1.CC(O)=O.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>ClC(Cl)C>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([CH2:7][N:8]([CH2:28][C:27]2[CH:30]=[CH:31][C:24]([O:23][CH3:22])=[CH:25][CH:26]=2)[C@@H:9]([C:14]2[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=2)[C:10]([O:12][CH3:13])=[O:11])=[CH:20][CH:21]=1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 0 °C
Procedure
To a solution of (S)-methyl 2-((4-methoxybenzyl)amino)-2-phenylacetate (1.6 g, 5.61 mmol) in anhydrous dichloroethane (20 mL) was added 4-methoxy benzaldehyde (0.76 g, 5.61 mmol) and few drops of HOAc. After 30 min, the reaction mixture was cooled to 0° C., sodium triacetoxy borohydride (2.38 g, 11.22 mmol) was added and the contents were allowed to stir at ambient temperature. After 2 h, the reaction was quenched with ice cold H2O (10 mL), and the organic contents were extracted with CH2Cl2 (2×25 mL). The combined organic extracts were washed with brine (1×20 mL), dried over Na2SO4, concentrated and the residue thus obtained was purified by flash column chromatography to afford the title compoundas pale yellow liquid (1.5 g, 66%). MS ES+APCI calc'd. for C25H27NO4 [M+H]+ 406. Found 406.
Workup
- waitAfter 2 h
- customthe reaction was quenched with ice cold H2O (10 mL)
- extractionthe organic contents were extracted with CH2Cl2 (2×25 mL)
- washThe combined organic extracts were washed with brine (1×20 mL)
- dry with materialdried over Na2SO4
- concentrationconcentrated
- customthe residue thus obtained
- customwas purified by flash column chromatography
Sources & evidence
- ORD record
- ord-8d14263a40c847cc86b8e4478216cb05
- Source dataset
- uspto-grants-2016_01
- Patent number
- US09233979B2
Reaction notes
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