Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Zopiclone | HCID 5735 | — |
| Reactant | Benzenesulfonic Acid | HCID 7371 | — |
| Reactant | Eszopiclone | HCID 969472 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (S)-Zopiclone Besylate | HCID 131729769 | 92.7% |
Reaction Steps
A 2000 mL reactor was charged with 10.0 g (S)-zopiclone and 400 mL tetrahydrofuran (THF). The contents were heated to 35° C. Into a 1000 mL reactor was charged 4.4 g benzenesulfonic acid and 400 mL THF, and stirred until a solution was formed. The acid solution was transferred slowly to the zopiclone solution. The reaction was cooled to 15° C. and stirred for 18 hr at 20-25° C. The reactor slurry was filtered and washed with THF in an appropriate filter. The wet cake was dried under vacuum at 60-65° C. and packaged in an appropriate container. Isolated yield=92.7%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08198278B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-90643e01e1524768b70e4ce2ac9f7ebc |
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| Source note | uspto-grants-2012_06 |
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