Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 57322276 | HCID 57322276 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86745756 | HCID 86745756 | 110.7% |
Reaction Steps
A solution of the dihydroxyester prepared in Step D (35 mg; 0.068 mmole) in ethanol (2 mL) was treated with 1N NaOH solution (68 l; 0.068 mmole) and the mixture stirred for 30 minutes at 23° C. The solvent was removed by evaporation in vacuo and the residue dissolved in water (2 mL) and lyophilized to afford 36 mg (100%) of the title compound; m.p.>110° C. decomp. [α]D25 =-22.2° (c=0.32, H2O). The 1H NMR and 13C NMR are identical to the (±)-erythro product prepared in Example 12.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05110940 |
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| Source dataset | uspto-grants-1992_05 |
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| ORD ID | ord-a06b2c6baf5e40e59ab92861412297ce |
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| Source note | uspto-grants-1992_05 |
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