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Tetrahydrofuran ethanol → (5-(2-Methyl-1,3-dioxolan-2-yl)isoxazol-3-yl)methanol

HRID 416275
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 416275
[CH3:1][C:2]1([C:7]2[O:11][N:10]=[C:9]([C:12](OCC)=[O:13])[CH:8]=2)[O:6][CH2:5][CH2:4][O:3]1.CCO.C1COCC1>O>[CH3:1][C:2]1([C:7]2[O:11][N:10]=[C:9]([CH2:12][OH:13])[CH:8]=2)[O:6][CH2:5][CH2:4][O:3]1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 21873804Tetrahydrofuran ethanolHCID 58930452Ethyl 5-(2-methyl-1,3-dioxolan-2-yl)isoxazole-3-carboxylate

Produkt 1

HCID 58930623(5-(2-Methyl-1,3-dioxolan-2-yl)isoxazol-3-yl)methanolAusbeute 93,5 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

To a solution of the dioxolane 318 (3.14 g, 13.8 mmol) in a 1:2 mixture of EtOH-THF (45 mL) NaBH4 (0.68 g, 18.0 mmol) was added. The reaction mixture was stirred at room temperature for 2 hours, treated with water and the organic solvents were evaporated. The aqueous phase was extracted with EtOAc and combined organic layers were successively washed with H2O and brine, dried over MgSO4 and concentrated under reduced pressure to afford the title compound as oil (2.39 g, 93% yield) which was used for next step without further purification. 1H NMR (DMSO-d6) δ (ppm): 6.43 (s, 1H), 5.47 (t, J=5.9 Hz, 1H), 4.47 (d, J=5.9 Hz, 2H), 4.06-4.02 (m, 2H), 3.94-3.90 (m, 2H), 1.66 (s, 3H). MS (m/z): 185.18 (calc) 186.1 (MH+) (found).

Aufarbeitung

  1. additionwas added
  2. customthe organic solvents were evaporated
  3. extractionThe aqueous phase was extracted with EtOAc
  4. washwere successively washed with H2O and brine
  5. dry with materialdried over MgSO4
  6. concentrationconcentrated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-8e8a4c86d271424093661981e0142f22
Quelldatensatz
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08088805B2

Notizen zur Reaktion

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