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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1586374Generated: November 3, 2026

Clarithromycin → Clarithromycin

https://huagongshe.com/reaction/1586374

Reaction equation

Participants

RoleNameHCIDCharge
ReactantClarithromycinHCID 84029—
SolventEthanolHCID 702—
ProductClarithromycinHCID 84029—
Product1-Hydroxyethyl radicalHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05945405
Source datasetuspto-grants-1999_08
ORD IDord-a59b96931cb74ed1ae7b4e2fc17e32c7
Source noteuspto-grants-1999_08