HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → Erythromycin 2'-acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Erythromycin B | HCID 9918244 | — |
| Product | Erythromycin 2'-acetate | HCID 114919 | — |
Reaction Steps
Into a 1.0 L one neck round bottom flask were placed 50 g of erythromycin B (69.64 m mole), 500 mL ethyl acetate and 16 mL acetic anhydride (17.3 g, 169.6 m mole). The solution was stirred at room temperature overnight. Copious amounts of white solids were observed. This mixture was filtered to give 26.2 g solid. The filtrate was washed with 300 mL 5% sodium bicarbonate twice, and the organic layer was dried with magnesium sulfate. The solvent was removed by vacuum distillation to give a second crop of desired product (22.3 g). The product was identified by mass spectroscopy and NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06194387B1 |
| Source dataset | uspto-grants-2001_02 |
| ORD ID | ord-cfc762903425465084b636c4057948a6 |
| Source note | uspto-grants-2001_02 |