StartseiteMCPWorkbenchSkills
StartseiteWorkbenchBenachrichtigungenMein Bereich
llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
  1. Startseite
  2. /Reaktion

Diisobutylaluminum hydride → 3-(4-Iodopyrazol-1-yl)-2,2-dimethylpropan-1-ol

HRID 2279839
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2279839
C[O:2][C:3](=O)[C:4]([CH3:13])([CH3:12])[CH2:5][N:6]1[CH:10]=[C:9]([I:11])[CH:8]=[N:7]1.CC(C[AlH]CC(C)C)C.[OH-].[NH4+]>C1COCC1>[I:11][C:9]1[CH:8]=[N:7][N:6]([CH2:5][C:4]([CH3:13])([CH3:12])[CH2:3][OH:2])[CH:10]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 14487Diisobutylaluminum hydrideHCID 14923Ammonium HydroxideHCID 678164023-(4-Iodopyrazol-1-yl)-2,2-dimethylpropionic acid methyl ester2×

Produkt 1

HCID 678114803-(4-Iodopyrazol-1-yl)-2,2-dimethylpropan-1-ol

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

A cold (−20° C.) solution of 3-(4-Iodopyrazol-1-yl)-2,2-dimethylpropionic acid methyl ester (Compound 47F, 6.0 g, 19.48 mmol) in THF (80 mL) was treated with DIBAL (42.85 mL, 42.85 mmol, 1M solution in toluene) and allowed to warm to RT over a period of 2 h. The reaction mixture was treated with aq. ammonium hydroxide (20 mL) and the solids were filtered through celite. The filtrate was diluted with ethyl acetate (50 mL) and washed with brine (2×50 mL). The organic layer was dried over Na2SO4, filtered and concentrated to give 4.9 g (90%) as an oil which crystallized upon standing. 1H NMR (500 MHz, CDCl3) δ 7.50 (s, 1H), 7.41 (s, 1H), 4.0 (s, 2H), 3.17 (s, 3H), 0.9 (s, 6H).

Aufarbeitung

  1. filtrationthe solids were filtered through celite
  2. additionThe filtrate was diluted with ethyl acetate (50 mL)
  3. washwashed with brine (2×50 mL)
  4. dry with materialThe organic layer was dried over Na2SO4
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customto give 4.9 g (90%) as an oil which
  8. customcrystallized

Quellen und Nachweise

ORD-Eintrag
ord-430cd4f409054bbda8a82a80d11ba53e
Quelldatensatz
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09133224B2

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion