HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 267502Generated: November 1, 2026
Sodium Hydroxide → HCID 178521533, compound
https://huagongshe.com/reaction/267502
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | [(Trifluoromethyl)sulfanyl]acetyl chloride | HCID 15733943 | — |
| Reactant | HCID 178508106 | HCID 178508106 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 178521533 | HCID 178521533 | — |
Reaction Steps
To a cold solution (-20°) of 7-amino-3-(5-hydroxy-1,2,4-triazol-3-ylthiomethyl)-3-cephem-4-carboxylic acid (3.39 g., 0.01 mole) in a mixture of acetone (62.5 ml.) and 3% NaHCO3 (62.5 ml.) is added dropwise over a 30 minute period a solution of trifluoromethylmercaptoacetyl chloride (2.24 g., 0.012 mol.) in acetone (20 ml.) The solution is maintained at pH 8 by adding 10% sodium hydroxide as needed. The reaction is stirred for 20 minutes at -15° to -20° and then allowed to warm to room temperature. The solution is washed with ether, covered with ethyl acetate and acidified to pH 2. The aqueous phase is separated and extracted with ethyl acetate. The combined ethyl acetate phases are combined, washed with water, dried, and evaporated to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03943131 |
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| Source dataset | uspto-grants-1976_03 |
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| ORD ID | ord-a3dd9d8e70aa4c23a4250c490d4adeff |
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| Source note | uspto-grants-1976_03 |
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