Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cephalexin | HCID 27447 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | Cephalexin Monohydrate | HCID 62921 | — |
Reaction Steps
IPA (16 liters) was added to the aqueous phase and the pH was slowly lowered to 7.7 by acid addition [step (e)]. The system was seeded with cephalexin and, after crystallization began, the pH was lowered in 0.1 pH unit increments by acid addition to pH 7.0 [step (f)], and finally to pH 5.0 [step (h)]. The crystal slurry was chilled to 1° C. for 1 hour [step (g)], then centrifuged to obtain a cephalexin monohydrate product [step (h)].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05034522 |
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| Source dataset | uspto-grants-1991_07 |
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| ORD ID | ord-d6e5cb56217c42d09ba0764af2c6af55 |
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| Source note | uspto-grants-1991_07 |
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