Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Clarithromycin | HCID 84029 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Clarithromycin | HCID 84029 | — |
| Product | 1-Hydroxyethyl radical | HCID 119440 | — |
Reaction Steps
A mixture of 6-O-methylerythromycin A (20 g), prepared as described above, and ethanol (200 mL) was warmed to reflux and the insoluble material (11.2 g) was removed by filtration. The filtrate was transferred to a clean flask and heated to reflux. The clear solution was allowed to cool to ambient temperature and then was further cooled in an ice bath. The liquid was decanted to leave 6-O-methylerythromycin A form 0 ethanolate which was sealed in a container without further drying. The 2-theta angle positions in the single crystal x-ray diffraction pattern of 6-O-methylerythromycin A form 0-ethanolate are 4.72°±0.2, 6.60°±0.2, 7.72°±0.2, 9.30°±0.2, 10.40°±0.2, 11.10°±0.2, 11.86°±0.2, 12.72°±0.2, 13.90°±0.2, 15.02°±0.2, 17.18°±0.2, 18.50°±0.2, 19.08°±0.2, 19.68°±0.2, 23.14°±0.2 and 23.98°±0.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05945405 |
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| Source dataset | uspto-grants-1999_08 |
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| ORD ID | ord-a59b96931cb74ed1ae7b4e2fc17e32c7 |
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| Source note | uspto-grants-1999_08 |
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