HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → HCID 131712368, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 131712369 | HCID 131712369 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 131712368 | HCID 131712368 | — |
Reaction Steps
A mixture of 21 g of the product of Step A, 80 ml of acetone and 27 ml of 2 N hydrochloric acid was stirred at room temperature for 90 minutes and 55 ml of water were added thereto with stirring. The acetone was evaporated under reduced pressure and 140 ml of ethyl acetate were added with stirring. The decanted aqueous phase was extracted with ethyl acetate and the combined organic phases were washed with half saturated aqueous sodium chloride solution, was dried and vacuum filtered to obtain the syn isomer of 3-methyl-7-[2-(2-tritylamino-4-thiazolyl)-2-hydroxyiminoacetamido]-ceph-3-eme-4-carboxylic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04374834 |
| Source dataset | uspto-grants-1983_02 |
| ORD ID | ord-f28b83d549144206aad5ddab9426ad7f |
| Source note | uspto-grants-1983_02 |