HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2413412Generated: November 2, 2026
Trifluoroacetic acid → HCID 13175970, compound
https://huagongshe.com/reaction/2413412
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 13175940 | HCID 13175940 | — |
| Product | HCID 13175970 | HCID 13175970 | 100.8% |
Reaction Steps
2-Benzhydryloxycarbonyl-7-t-butoxycarbonylamino-8-oxo-3-(2-phenyl-thiazol-5-yl)-5-thia-1-azabicyclo[4.2.0]-oct-2-ene (5.7 g) is treated with trifluoroacetic acid (57 cc) for 20 minutes at 20° C. and the reaction mixture is then concentrated to dryness under reduced pressure (0.2 mm Hg; 0.03 kPa) at 30° C. The residue is taken up in ethyl acetate (100 cc), which is evaporated under reduced pressure (30 mm Hg; 4 kPa) at 30° C. This residue is triturated with isopropyl ether (100 cc). The solid is filtered off, washed with isopropyl ether (3×50 cc) and dried under reduced pressure (0.2 mm Hg; 0.03 kPa) at 20° C. 7-Amino-2-carboxy-8-oxo-3-(2-phenyl-thiazol-5-yl)-5-thia-1-azabicyclo[4.2.0]oct-2-ene (3.3 g) is obtained in the form of an ochre solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04496560 |
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| Source dataset | uspto-grants-1985_01 |
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| ORD ID | ord-841a861d7bfb4a9f91a0ebc3fadd13dc |
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| Source note | uspto-grants-1985_01 |
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