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Acetone → 4-(5-Chloro-2-methoxyphenyl)-3-buten-2-one

HRID 1700711
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1700711
[OH-].[Na+].[Cl:3][C:4]1[CH:5]=[CH:6][C:7]([O:12][CH3:13])=[C:8]([CH:11]=1)[CH:9]=O.[CH3:14][C:15]([CH3:17])=[O:16]>O>[Cl:3][C:4]1[CH:5]=[CH:6][C:7]([O:12][CH3:13])=[C:8]([CH:9]=[CH:14][C:15](=[O:16])[CH3:17])[CH:11]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 180Acetone2×HCID 14798Sodium HydroxideHCID 37183565-Chloro-2-methoxybenzaldehyde

Produkt 1

HCID 536609684-(5-Chloro-2-methoxyphenyl)-3-buten-2-one

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

In water (100 ml) was dissolved sodium hydroxide (3.0 g), and to the solution was added acetone (80 ml) and then was added dropwise a solution of 5-chloro-2-methoxybenzaldehyde (11.8 g) in acetone (30 ml). The reaction solution was stirred at room temperature for 2 hours, and acetone was evaporated under reduced pressure. The residue was extracted with ethyl acetate, and the organic layer was washed with water and saturated brine and concentrated under reduced pressure. The residue was purified with silica gel column chromatography to give 4-(5-chloro-2-methoxyphenyl)-3-buten-2-one (6.8 g).

Aufarbeitung

  1. customacetone was evaporated under reduced pressure
  2. extractionThe residue was extracted with ethyl acetate
  3. washthe organic layer was washed with water and saturated brine
  4. concentrationconcentrated under reduced pressure
  5. customThe residue was purified with silica gel column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-ab7cdc2fdce54d36b9569af9c2294b54
Quelldatensatz
uspto-grants-2002_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06350749B1

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