Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Simvastatin phenylboronate | HCID 86757524 | — |
| Solvent | 1,3-Propanediol | HCID 10442 | — |
| Product | Simvastatin | HCID 54454 | 90.1% |
Reaction Steps
A suspension of simvastatin phenylboronate (30.0 g) and 1,3-propanediol (450 mL) was heated at 105 to 107° C. at 0.2 mm Hg. After 1 hour, 182 mL of distillate was collected and the reaction was cooled to 20 to 25° C. Deionized water (270 mL) was added and toluene (3×75 mL) was used to extract the mixture. The combined toluene layers were washed with water (2×30 mL). The organic solution was heated at reflux for 1 hour and water was azeotropically removed. The solution was concentrated to a final volume of 24 mL under vacuum at 48 to 50° C. To the concentrated solution was added hexanes (215 mL) over 10 minutes. The resulting slurry was cooled to 0 to 5° C. and filtered. The crude simvastatin was washed with 0 to 5° C. hexanes and dried under vacuum to yield 21.0 g (88%) of simvastatin.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06307066B1 |
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| Source dataset | uspto-grants-2001_10 |
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| ORD ID | ord-fe2a5176415440fabeb54a35884ccec3 |
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| Source note | uspto-grants-2001_10 |
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