Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Chloromethyl pivalate | HCID 87885 | — |
| Reactant | HCID 56979190 | HCID 56979190 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86608983 | HCID 86608983 | — |
Reaction Steps
At room temperature (25° C.), 1.35 g (4.0 mmol) of (3S,4S)-1-carboxymethyl-4-[(1R)-1-(phenylthiocarbonyl)ethyl]-3-[(1R)-1-hydroxyethyl]-2-azetidinone was dissolved in 8 ml of dimethylformamide, and 1.20 (8.0 mmol) of-pivaloyloxymethyl chloride and 1.20 g (8.0 mmol) of sodium iodide were sequentially added thereto. Subsequently, 0.68 g (5.3 mmol) of diisopropylethylamine was added dropwise thereto, and stirring was performed at the same temperature for 6 hours. The reaction solution was diluted with 40 ml of ethyl acetate, and washing was performed several times using 5% aqueous sodium bicarbonate and water. The resulting ethyl acetate solution was dried over sodium sulfate, and then the solvent was removed by distillation. Thereby, 1.88 g of the target compound was produced.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07538212B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-0857b51058d447e0bbe8ea23cc7a8ed6 |
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| Source note | uspto-grants-2009_05 |
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