HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 596843Generated: October 31, 2026
Hydrochloric Acid → HCID 70636145, compound
https://huagongshe.com/reaction/596843
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 88777142 | HCID 88777142 | — |
| Reactant | HCID 178418443 | HCID 178418443 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 70636145 | HCID 70636145 | 30.6% |
Reaction Steps
To a cooled (-73° C.), stirred solution of 1.559 g. of benzhydryl 7-(2-thienylacetamido)-3-formyl-2-cephem-4-carboxylate and 20 ml. of dry tetrahydrofuran was added 3.13 ml. of 2.88 M. ethyl magnesium bromide. After the reaction mixture was allowed to stir for four minutes at -73° C., 10 ml. of 1N.HCl was added and the solution allowed to warm to 0° C. The reaction mixture was transferred to a separatory funnel with the aid of cold ethyl acetate and cold 1N.HCl. The organic layer was separated and washed twice with cold 1N.HCl and twice with brine and then dried over anhydrous sodium sulfate. Evaporation in vacuo to dryness provided a product residue which was chromatographed on silica gel using a toluene-ethyl acetate gradient to give 0.140 g. of the starting 3-formyl-2-cephem ester and 0.507 g. (30.6 percent) of the title product as a mixture of diasteromers:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04012380 |
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| Source dataset | uspto-grants-1977_03 |
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| ORD ID | ord-e4f5ddd6e0e34fef81046c8671477ac0 |
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| Source note | uspto-grants-1977_03 |
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