HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1858515Generated: November 2, 2026
Trifluoroacetic acid → HCID 178525231, compound
https://huagongshe.com/reaction/1858515
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Anisole | HCID 7519 | — |
| Reactant | Diisopropyl Ether | HCID 7914 | — |
| Reactant | HCID 131722162 | HCID 131722162 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178525231 | HCID 178525231 | 77.4% |
Reaction Steps
To a mixture of benzhydryl 7β-(2-phenylacetamido)-3-(4-carboxymethylthiazol-2-yl)thio-3-cephem-4-carboxylate potassium salt (1.10 g), anisole (1.10 ml) and dichloromethane (3.30 ml) was added trifluoroacetic acid (2.20 ml) at 15° C. After stirring at room temperature for 1 hour, the solution was poured into diisopropyl ether. The resulting precipitate was collected by filtration, added to a mixture of tetrahydrofuran and water and adjusted to pH 7.2 with an aqueous sodium bicarbonate. The separated aqueous solution was adjusted to pH 3.0 with 1N-hydrochloric acid and extracted with tetrahydrofuran. The tetrahydrofuran solution was washed with saturated sodium chloride solution, dried over magnesium sulfate and evaporated under reduced pressure. Ethyl acetate was added to the residue and the resulting crystal was collected by filtration to give 7β-(2-phenylacetamido)-3-(4-carboxymethylthiazol-2-yl)thio-3-cephem-4-carboxylic acid (595 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06150351 |
|---|
| Source dataset | uspto-grants-2000_11 |
|---|
| ORD ID | ord-2fa103931b4040aebb3e3cabc9002822 |
|---|
| Source note | uspto-grants-2000_11 |
|---|