HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 336212Erstellt: 25. Oktober 2026
Hexamethylphosphoramide → HCID 10961504, Verbindung
https://huagongshe.com/reaction/336212
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hexamethylphosphoramide | HCID 12679 | — |
| Edukt | 1-Chloro-5-iodopentane | HCID 108914 | — |
| Edukt | tert-butyl (2R,3S)-6-oxo-2,3-diphenylmorpholine-4-carboxylate | HCID 981230 | — |
| Edukt | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | HCID 10961504 | HCID 10961504 | — |
Reaktionsschritte
A 1.0M solution of sodium bis(trimethylsilyl)amide in THF (55.0 mL, 55.2 mmol) is added at −78° C. to a solution of (5S,6R)-5,6-diphenyl-4-tert-butoxycarbonyl-morpholin-2-one (13.0 g, 36.8 mmol), 1-chloro-5-iodo-pentane (25.0 g, 108.0 mmol) and HMPA (55.0 mL) in THF (200.0 mL). The reaction mixture is stirred at −78° C. for 2 hours and at room temperature for 1 hour. The reaction mixture is diluted with EtOAc, washed with water and brine. After drying the organic phase over anhydrous Na2SO4, the solvent is removed under reduced pressure to afford the crude product that is purified by silica gel column chromatography to afford the title compound; m/z 358 [M-Boc+H].
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08889670B2 |
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| Quelldatensatz | uspto-grants-2014_11 |
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| ORD ID | ord-a314b8452555435e9290bcb694219f81 |
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| Quellennotiz | uspto-grants-2014_11 |
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