Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Barium hydroxide | HCID 6093286 | — |
| Reactant | HCID 14348480 | HCID 14348480 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 14348570 | HCID 14348570 | — |
Reaction Steps
A mixture (140 mg) of the isomers (10a) and (10b) of diethyl 2-(1-hydroxyethyl)-3-benzylamino-4-methylpentanedioate (10a:10b=5:2) as obtained in Example 14 (2.15 g) was dissolved in tetrahydrofuran (4 ml), barium hydroxide (250 mg) and water (2 ml) were added thereto, and the resultant mixture was stirred vigorously at room temperature of 45 minutes. Insoluble materials were collected by filtration and washed with ethanol. The washing and the filtrate were combined together and concentrated under reduced pressure. The residue was subjected to thin layer chromatography, whereupon a new spot was revealed in addition to the spots corresponding to the starting material and the original point. The product as the new spot was collected and fractionally purified to give (2RS,3RS,4SR,5SR)-2-methyl-3-benzylamino-4-ethoxycarbonyl-5-hydroxyhexanoic acid (70 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05134231 |
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| Source dataset | uspto-grants-1992_07 |
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| ORD ID | ord-d475fa2d81dc498fa2f2bbd644792493 |
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| Source note | uspto-grants-1992_07 |
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