HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569441Generated: October 29, 2026
Trifluoroacetic acid → HCID 131713348, compound
https://huagongshe.com/reaction/569441
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Anisole | HCID 7519 | — |
| Reactant | Diisopropyl Ether | HCID 7914 | — |
| Reactant | HCID 131713349 | HCID 131713349 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 131713348 | HCID 131713348 | 74.4% |
Reaction Steps
Trifluoroacetic acid (5.75 g) was added to a solution of pivaloyloxymethyl 7-[2-(2-aminothiazol-4-yl)-2-benzhydryloxycarbonylmethoxyiminoacetamido]-3-vinyl-3-cephem-4-carboxylate (syn isomer) (3.7 g) in methylene chloride (14.8 ml) and anisole (1.09 g) under ice-cooling, and the mixture was stirred for an hour at ambient temperature. Then the reaction mixture was added dropwise to diisopropyl ether (160 ml). The precipitates were collected by filtration and washed with diisopropyl ether, followed by adding them to a mixture of water (60 ml) and ethyl acetate (60 ml). The resultant mixture was adjusted to pH 7.0 with a saturated aqueous sodium bicarbonate. The separated aqueous solution was further adjusted to pH 2.5 with 10% hydrochloric acid. The precipitates were collected by filtration, washed with water and then dried over phosphorus pentoxide in vacuo to give pivaloyloxymethyl 7-[2-(2-aminothiazol-4-yl)-2-carboxymethoxyiminoacetamido]-3-vinyl-3-cephem-4-carboxylate (syn isomer) (2.13 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04731443 |
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| Source dataset | uspto-grants-1988_03 |
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| ORD ID | ord-68c508672d3546b2a2b257618106bba9 |
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| Source note | uspto-grants-1988_03 |
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