HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1733204Generated: November 1, 2026
Sodium Iodide → Pivaloyloxymethyl (3S, 5R)-penam-3-carboxylate 1,1-Dioxide
https://huagongshe.com/reaction/1733204
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Chloromethyl pivalate | HCID 87885 | — |
| Reactant | (3S, 5R)-penam-3-carboxylic acid 1,1-dioxide | HCID 13518352 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Pivaloyloxymethyl (3S, 5R)-penam-3-carboxylate 1,1-Dioxide | HCID 86737398 | — |
Reaction Steps
To a stirred solution of 2.05 g of (3S, 5R)-penam-3-carboxylic acid 1,1-dioxide in 10 ml of N,N-dimethylformamide is added 1.30 g of diisopropylethylamine followed by 1.50 g of chloromethyl pivalate and 50 mg of sodium iodide at ca. 0° C. The reaction mixture is stirred at ca. 0° C. for 30 minutes and then at room temperature for 24 hours. The reaction mixture is then diluted with ethyl acetate and water and the pH of the aqueous phase is adjusted to 7.5. The ethyl acetate layer is separated and washed three times with water and once with saturated sodium chloride solution. The ethyl acetate solution is then dried using anhydrous sodium sulfate, and evaporated in vacuo to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04241050 |
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| Source dataset | uspto-grants-1980_12 |
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| ORD ID | ord-c16c55450f084c09aa36520f2e2942bf |
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| Source note | uspto-grants-1980_12 |
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