HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 237155Generated: October 29, 2026
Dimethylformamide → HCID 178514770, compound
https://huagongshe.com/reaction/237155
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 2-(2,2,2-Trifluoroethanesulfinyl)acetic acid | HCID 20574023 | — |
| Reactant | HCID 178508099 | HCID 178508099 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 178514770 | HCID 178514770 | — |
Reaction Steps
A suspension of 4.17 g. (0.01 mol.) of 7-amino-3-[1-(2-sulfamoylethyl)tetrazol-5-ylthiomethyl]-3-cephem-4-carboxylic acid in 50 ml. of dry dimethylformamide is treated with 2 ml. of triethylamine and the mixture is stirred for 15 minutes at 25°. A slight excess of 0.01 mol. of the activated ester of 2,2,2-trifluoroethylsulfinylacetic acid is added to the mixture and it is stirred an additional hour. The reaction mixture is evaporated to dryness and water and ethyl acetate are added to the residue. The layers are separated, ethyl acetate is added to the aqueous phase and it is acidified to pH 2.5 by addition of 6 N hydrochloric acid. The mixture is filtered, the layers are separated and the aqueous phase is extracted with ethyl acetate. The extract is washed with water, dried (MgSO4) and evaporated to dryness to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04159373 |
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| Source dataset | uspto-grants-1979_06 |
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| ORD ID | ord-2f1c09c5c1f7439fa40b716676ef9bfd |
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| Source note | uspto-grants-1979_06 |
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