Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2413412Generated: November 2, 2026

Trifluoroacetic acid → HCID 13175970, compound

https://huagongshe.com/reaction/2413412

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 13175940HCID 13175940—
ProductHCID 13175970HCID 13175970100.8%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04496560
Source datasetuspto-grants-1985_01
ORD IDord-841a861d7bfb4a9f91a0ebc3fadd13dc
Source noteuspto-grants-1985_01