HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 237158Generated: October 29, 2026
Sodium Hydroxide → HCID 178460997, compound
https://huagongshe.com/reaction/237158
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Methylthioacetyl chloride | HCID 21249692 | — |
| Reactant | HCID 178508099 | HCID 178508099 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 178460997 | HCID 178460997 | — |
Reaction Steps
To a stirred, cooled (-20°) solution of 10.8 g. (0.026 mol.) of 7-amino-3-[1-(2-sulfamoylethyl)tetrazol-5-ylthiomethyl]-3-cephem-4-carboxylic acid in 220 ml. of 3% sodium bicarbonate and 220 ml. of acetone is dropwise added a solution of 3.66 g. (0.029 mol.) of methylthioacetyl chloride in 52 ml. of acetone, during which time the pH of the reaction mixture is maintained at 8.0 by addition of 10% sodium hydroxide. After addition the reaction mixture is stirred an additional 20 minutes at -15°, then is warmed to 25° and extracted with ether. The remaining aqueous phase is cooled, 250 ml. of ethyl acetate is added and the slurry is acidified with 3 N hydrochloric acid. The layers are separated and the aqueous phase is extracted twice more with ethyl acetate. The combined extracts are dried (MgSO4) and evaporated to dryness to yield 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-54908d6741184918918addd23e44f83b |
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| Source note | uspto-grants-1979_06 |
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