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Lithium hydroxide, monohydrate → tert-butyl(E)-5-chloro-2-{1-[3-fluoro-4-(4-methyl-1H-imidazol-1-yl)phenyl]methylidene}valerate

HRID 1436138
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1436138
[F:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][C:9]=1[N:10]1[CH:14]=[C:13]([CH3:15])[N:12]=[CH:11]1)[CH:5]=O.[Cl:16][CH2:17][CH2:18][CH2:19][CH:20](P(OCC)(OCC)=O)[C:21]([O:23][C:24]([CH3:27])([CH3:26])[CH3:25])=[O:22].O.[OH-].[Li+].O.C(=O)(O)[O-].[Na+]>C1COCC1.C(O)C>[Cl:16][CH2:17][CH2:18][CH2:19]/[C:20](=[CH:5]\[C:4]1[CH:7]=[CH:8][C:9]([N:10]2[CH:14]=[C:13]([CH3:15])[N:12]=[CH:11]2)=[C:2]([F:1])[CH:3]=1)/[C:21]([O:23][C:24]([CH3:27])([CH3:26])[CH3:25])=[O:22]
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Komponenten

7

Edukt 4

HCID 168937Lithium hydroxide, monohydrateHCID 707008423-Fluoro-4-(4-methyl-1H-imidazol-1-yl)benzaldehydeHCID 86585896Sodium bicarbonate waterHCID 86602480Tert-butyl 5-chloro-2-(diethoxyphosphoryl)valerate

Produkt 1

HCID 69004836tert-butyl(E)-5-chloro-2-{1-[3-fluoro-4-(4-methyl-1H-imidazol-1-yl)phenyl]methylidene}valerate
Ausbeute 46,2 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 702EthanolLösungsmittelHCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

3-Fluoro-4-(4-methyl-1H-imidazol-1-yl)benzaldehyde (2.29 g) and tert-butyl 5-chloro-2-(diethoxyphosphoryl)valerate (3.68 g) were dissolved in a mixed solvent of THF (30 mL) and ethanol (10 mL). Lithium hydroxide monohydrate (1.41 g) was added to the reaction solution at room temperature, and the reaction solution was stirred at room temperature for 18 hours. Saturated sodium bicarbonate water was added to the reaction solution, followed by extraction with ethyl acetate. The resulting extract was dried over magnesium sulfate and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (elution solvent: heptane-ethyl acetate system), solidified with tert-butyl methyl ether and heptane, and separated by filtration to obtain 1.96 g of the title compound. The property values of the compound are as follows.

Aufarbeitung

  1. extractionfollowed by extraction with ethyl acetate
  2. extractionThe resulting extract
  3. dry with materialwas dried over magnesium sulfate
  4. concentrationconcentrated under reduced pressure
  5. customThe residue was purified by silica gel column chromatography (elution solvent: heptane-ethyl acetate system)
  6. customseparated by filtration

Quellen und Nachweise

ORD-Eintrag
ord-e4245d1eb6c94ba9994356168e0a6688
Quelldatensatz
uspto-grants-2009_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07618960B2

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