Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 24823937 | HCID 24823937 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 24822637 | HCID 24822637 | 30.3% |
Reaction Steps
To a solution of tert-butyl [2-(4-aminophenyl)-ethyl][(2R)-2-(3-chlorophenyl)-2-hydroxyethyl]carbamate (1.75 g) and formaldehyde (37% w/w solution in water, 390 μl) in 1,2-dichloroethane (20 ml) was added sodium triacetoxyborohydride (1.23 g), and the mixture was stirred at room temperature for 18 hours under nitrogen atmosphere. The resulting mixture was poured into a mixture of 1N sodium hydroxide and chloroform, and the mixture was stirred for 20 minutes. The organic layer was separated, washed with brine, dried over magnesium sulfate and evaporated under reduced pressure. The residue was purified by column chromatography on silica gel (hexane/ethyl acetate=2/1) to give tert-butyl [(2R)-2-(3-chlorophenyl)-2-hydroxyethyl](2-[4-(methylamino)phenyl]ethyl]carbamate (550 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07629366B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-6a7bbb7754e0466e9ad5e34d3c0b9323 |
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| Source note | uspto-grants-2009_12 |
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