HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 328064Generated: October 29, 2026
Hydrochloric Acid → HCID 178477385, compound
https://huagongshe.com/reaction/328064
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dichloroacetyl chloride | HCID 6593 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 7-Amino-3-(1-methyl-1H-tetrazol-5-ylthiomethyl)-3-cephem-4-carboxylic acid | HCID 178477381 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178477385 | HCID 178477385 | 34.2% |
Reaction Steps
7-Amino-3-(1-methyl-1H-tetrazol-5-ylthiomethyl)-3-cephem-4-carboxylic acid (3.28 g) was suspended in a mixture (60 ml) of water and acetone (1:1) and sodium bicarbonate was added to the suspension little by little to give a solution. Dichloroacetyl chloride (3 g) was added dropwise to the solution at -5° C under stirring and the mixture was stirred at the same temperature for 30 minutes. Ethyl acetate (50 ml) was added to the reaction mixture and the mixture was adjusted to pH 2 with diluted hydrochloric acid under stirring and filtered. The ethyl acetate layer was separated from the filtrate, washed with saturated aqueous sodium chloride, dried over magnesium sulfate and then treated with activated charcoal powder. Ethyl acetate was distilled off from the solution under reduced pressure. Ether was added to the residue and the mixture was stirred overnight. Precipitates were collected by filtration to give pale yellow powder of 7-dichloroacetamido-3-(1-methyl-1H-tetrazol-5-ylthiomethyl)-3-cephem-4-carboxylic acid (1.5 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04016160 |
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| Source dataset | uspto-grants-1977_04 |
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| ORD ID | ord-4c4d6b511c324f689adb9665bd3d87ed |
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| Source note | uspto-grants-1977_04 |
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