1,4-Dioxane hydrochloride → HCID 21137721, Verbindung

HRID 1358581Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1358581
[CH3:1][O:2][C:3](=[O:30])[C@H:4]([CH3:29])[NH:5][C:6]1[CH:11]=[CH:10][C:9]([O:12][CH2:13][C:14]([O:16]C(C)(C)C)=[O:15])=[CH:8][C:7]=1[C:21](=[O:28])[C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1.Cl.O1CCOCC1>O1CCOCC1>[CH3:1][O:2][C:3](=[O:30])[C@H:4]([CH3:29])[NH:5][C:6]1[CH:11]=[CH:10][C:9]([O:12][CH2:13][C:14]([OH:16])=[O:15])=[CH:8][C:7]=1[C:21](=[O:28])[C:22]1[CH:23]=[CH:24][CH:25]=[CH:26][CH:27]=1

Komponenten

4

Versuchsvorschrift

A mixture of 4-t-butoxycarbonylmethoxy-N-(2-benzoylphenyl)alanine methyl ester (1.4 g), 4N hydrogen chloride/dioxane (10 ml) and dioxane (10 ml) was stirred at room temperature for 3 hours and allowed to stand overnight. The reaction mixture was concentrated under reduced pressure. To the residue was added toluene and the mixture was concentrated under reduced pressure. The residue was chromatographed on a silica gel column (LiChroprepDIOL (Merck)) using hexane: ethyl acetate=2:1−1:1 as the eluant to afford the title compound (0.87 g, Rf=0.53: thin layer chromatography on a silica gel plate using hexane: ethyl acetate=3:2 as the eluant).

Aufarbeitung

  1. waitto stand overnight
  2. concentrationThe reaction mixture was concentrated under reduced pressure
  3. additionTo the residue was added toluene
  4. concentrationthe mixture was concentrated under reduced pressure
  5. customThe residue was chromatographed on a silica gel column (LiChroprepDIOL (Merck))

Quellen und Nachweise

ORD-Eintrag
ord-09c6ccdd961e4b6d9517a89f30f242e2
Quelldatensatz
uspto-grants-2003_07
Patentnummer
US06596751B2

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