HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 647740Generated: October 29, 2026
Trifluoroacetic acid → HCID 67859710, compound
https://huagongshe.com/reaction/647740
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Anisole | HCID 7519 | — |
| Reactant | Diisopropyl Ether | HCID 7914 | — |
| Reactant | HCID 67859952 | HCID 67859952 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67859710 | HCID 67859710 | 25.2% |
Reaction Steps
To a suspension of benzhydryl 7-[2-(5-tritylamino-1,3,4-thiadiazol-2-yl)acetamido]-3-vinyl-3-cephem-4-carboxylate (2.6 g) in methylene chloride (30 ml) and anisole (2.1 g) was added trifluoroacetic acid (7.6 g) under ice-cooling, followed by stirring at ambient temperature for 1.5 hours. The reaction mixture was poured into diisopropyl ether (300 ml), and the precipitates were collected by filtration and suspended in water (40 ml). After adjusting to pH 7 with 10% aqueous sodium hydroxide, the aqueous solution was washed with ethyl acetate and then adjusted to pH 5 with 10% hydrochloric acid. The organic solvent included in the resultant aqueous solution was completely removed by evaporation, and the resultant aqueous solution was adjusted to pH 4 with dilute acetic acid, which was chromatographed on a non-ionic adsorption resin "Diaion HP-20" (50 ml). After washing with water, elution was carried out with 30% isopropyl alcohol, and the fractions containing a desired compound were collected and then concentrated under reduced pressure. The concentrate was lyophilized to obtain 7-[2-(5-amino-1,3,4-thiadiazol-2-yl)-acetamido]-3-vinyl-3-cephem-4-carboxylic acid (0.31 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04409214 |
|---|
| Source dataset | uspto-grants-1983_10 |
|---|
| ORD ID | ord-9d2fa8544c9f47748b0b48f9822173cd |
|---|
| Source note | uspto-grants-1983_10 |
|---|