HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 70106Erstellt: 24. Oktober 2026
Methyl iodide → (2S)-2-(((tert-butoxy)carbonyl)amino)-3-methoxypropanoic acid
https://huagongshe.com/de/reaction/70106
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methyl iodide | HCID 6328 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | N-[tert-butoxycarbonyl]-L-serine | HCID 98766 | — |
| Edukt | Sodium ethoxide | HCID 2723922 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | (2S)-2-(((tert-butoxy)carbonyl)amino)-3-methoxypropanoic acid | HCID 7016354 | — |
Reaktionsschritte
Under nitrogen a mixture of 74 ml abs. THF and 6 ml abs. methanol is cooled to −70° C. and 2 g sodium hydride (55-65% dispersion) are added. The suspension is stirred for 0.4 hour at ambient temperature. Under nitrogen, 2.05 g N-Boc-L-serine are suspended in 100 ml abs. THF and 40 ml of the prepared sodium ethoxide solution are added. The suspension is stirred for 1 hour at ambient temperature and 1 ml methyliodide are added. After 1 hour the remainder of the sodium ethoxide solution and another 2 ml of methyliodide are added. After 18 hours the reaction mixture is evaporated to dryness. The residue is washed with water and ether and extracted. The water phase is acidified and extracted with ethyl acetate and dichloromethane. 0.52 g of the product are obtained.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08822474B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-1a7854345f3e4da0922298bdc2c9bd38 |
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| Quellennotiz | uspto-grants-2014_09 |
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