HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1064949Erstellt: 24. Oktober 2026
(S)-4-Benzyl-3-(ethoxyacetyl)oxazolidin-2-one → HCID 69279901, Verbindung
https://huagongshe.com/de/reaction/1064949
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | (S)-4-Benzyl-3-(ethoxyacetyl)oxazolidin-2-one | HCID 10825429 | — |
| Edukt | 4-Benzyloxy-2-(trifluoromethyl)benzaldehyde | HCID 22273885 | — |
| Edukt | HCID 178418657 | HCID 178418657 | — |
| Lösungsmittel | Triethylamine | HCID 8471 | — |
| Produkt | HCID 69279901 | HCID 69279901 | — |
Reaktionsschritte
In analogy to the procedure described in example 1 a], (S)-4-benzyl-3-ethoxyacetyl-oxazolidin-2-one (for the preparation of (S)-4-benzyl-3-ethoxyacetyl-oxazolidin-2-one see: D. Haigh, H. C. Birrell, B. C. C. Cantello, D. S. Eggleston, R. C. Haltiwanger, R. M. Hindley, A. Ramaswamy, N. C. Stevens, Tetrahedron: Asymmetry 1999, 10, 1353-1367) was reacted with 4-benzyloxy-2-trifluoromethyl-benzaldehyde in the presence of triethylamine and di-n-butylboron triflate to give (S)-4-benzyl-3-[(2S,3R)-3-(4-benzyloxy-2-trifluoromethyl-phenyl)-2-ethoxy-3-hydroxy-propionyl]-oxazolidin-2-one as colorless liquid. According to 1H-NMR spectroscopy, one of the four isomers is strongly predominating. The configuration was tentatively assigned as 2S,3R according to D. Haigh et al., Tetrahedron: Asymmetry 1999, 10, 1353-1367.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06969725B2 |
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| Quelldatensatz | uspto-grants-2005_11 |
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| ORD ID | ord-5e14ff88f7014ad287707ab08f759c17 |
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| Quellennotiz | uspto-grants-2005_11 |
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