Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl Acrylate | HCID 8821 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 11435600 | HCID 11435600 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 86592536 | HCID 86592536 | 43.7% |
Reaction Steps
To a solution of methyl (3S)-3-{[(allyloxy)carbonyl]amino}butanoate (2.06 g, 10.2 mmol) and ethyl acrylate (1.11 ml, 10.2 mmol) in toluene (25 ml) was added at 40° C. sodium hydride (60% suspension in oil, 0.41 g, 10.2 mmol). The mixture was stirred for 2 hours and then was poured into diluted hydrochloric acid. The solution was extracted twice with ethyl acetate. The organic layer was washed with a saturated aqueous sodium chloride solution and dried over magnesium sulfate. The organic solvent was removed in vacuo. To the residue were added methanol (40 ml), acetic acid (0.70 ml, 12.2 mmol) and sodium cyanoborohydride (0.77 g, 12.2 mmol) and the mixture was stirred at room temperature for 20 minutes. The solvent was removed in vacuo and the residue was purified with silica gel chromatography to give a mixture (1.21 g) of 1-allyl 3-ethyl (6S)-4-hydroxy-6-methyl-1,3-piperidinedicarboxylate and 1-allyl 3-methyl (6S)-4-hydroxy-6-methyl-1,3-piperidinedicarboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07163936B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-44d5155f16e240ebaeedc5907d8e3f8e |
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| Source note | uspto-grants-2007_01 |
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