Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Calcium Chloride | HCID 5284359 | — |
| Reactant | HCID 66974953 | HCID 66974953 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66976007 | HCID 66976007 | 83.1% |
Reaction Steps
To a suspension of calcium chloride (27.6 g) in THF (234 mL) and ethanol (176 mL) was added, under a nitrogen stream, sodium borohydride (12.5 g), and the mixture was stirred at room temperature for 1 hr. To the reaction mixture was added a solution of methyl (2RS,3RS)-2-[(benzylamino)methyl]-3-(4-chloro-3-fluorophenyl)-3-hydroxypropanoate (58.2 g) in THF (200 mL) and ethanol (150 mL) under ice-cooling, and the mixture was stirred at room temperature for 5 hr. To the reaction mixture was added 6 N aqueous hydrochloric acid solution (28 ml), the mixture was neutralized with 8 N aqueous sodium hydroxide solution, and the mixture was filtered through celite. The obtained oil was diluted with ethyl acetate, and the diluted solution was washed with distilled water and brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to give the title compound (44.5 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08722662B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-8316f730db7a4f0ba1c68a3e40009e64 |
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| Source note | uspto-grants-2014_05 |
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