Cyclohexanecarboxaldehyde → 4-(1-Formyl-cyclohexyl)-but-2-enoic acid methyl ester

HRID 2070553

Reaktionsgleichung

Reaktionsgleichung von HRID 2070553
[CH:1]1([CH:7]=[O:8])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[CH3:9][O:10][C:11](=[O:16])[CH:12](O)[CH:13]=[CH2:14].O.C1(C)C=CC(S(O)(=O)=O)=CC=1>C1(C)C=CC=CC=1>[CH3:9][O:10][C:11](=[O:16])[CH:12]=[CH:13][CH2:14][C:1]1([CH:7]=[O:8])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1

Komponenten

5

Edukt 3

HCID 16275CyclohexanecarboxaldehydeHCID 521998p-Toluenesulfonic acid monohydrateHCID 545123Methyl 2-hydroxybut-3-enoate

Produkt 1

HCID 727655614-(1-Formyl-cyclohexyl)-but-2-enoic acid methyl ester

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1140TolueneLösungsmittel

Versuchsvorschrift

To a solution of cyclohexanecarbaldehyde (6.3 mL) and 2-hydroxy-3-butenoic acid methyl ester (5 mL) in toluene (40 mL) was added para-toluenesulfonic acid monohydrate (20 mg), and the reaction mixture was heated under reflux by using a Dean-Stark apparatus for 16.5 hours. After cooling down to room temperature, the reaction mixture was concentrated in vacuo. The residue was purified by column chromatography on silica gel (hexane:ethyl acetate (volume ratio)=50:1 to 10:1) to give 4-(1-formyl-cyclohexyl)-but-2-enoic acid methyl ester (3.7 g).

Aufarbeitung

  1. temperaturethe reaction mixture was heated
  2. temperatureunder reflux
  3. customfor 16.5 hours
  4. concentrationthe reaction mixture was concentrated in vacuo
  5. customThe residue was purified by column chromatography on silica gel (hexane:ethyl acetate (volume ratio)=50:1 to 10:1)

Quellen und Nachweise

ORD-Eintrag
ord-0e9cb1be9eef4ba38d47d16c36ec66cc
Quelldatensatz
uspto-grants-2012_10
Patentnummer
US08299296B2

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