3-Chloro-4-methylaniline → 3-chloro-N-cyclohexylmethyl-4-methylaniline

HRID 1368243Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1368243
[Cl:1][C:2]1[CH:3]=[C:4]([CH:6]=[CH:7][C:8]=1[CH3:9])[NH2:5].[CH:10]1([CH:16]=O)[CH2:15][CH2:14][CH2:13][CH2:12][CH2:11]1.C([BH3-])#N.[Na+]>CO>[Cl:1][C:2]1[CH:3]=[C:4]([CH:6]=[CH:7][C:8]=1[CH3:9])[NH:5][CH2:16][CH:10]1[CH2:15][CH2:14][CH2:13][CH2:12][CH2:11]1

Komponenten

5

Edukt 3

HCID 72553-Chloro-4-methylanilineHCID 16275CyclohexanecarboxaldehydeHCID 5003444Sodium cyanoborohydride

Produkt 1

HCID 224851623-chloro-N-cyclohexylmethyl-4-methylanilineAusbeute 85,3 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

To a solution of 3-chloro-4-methylaniline (7.08 g) in methanol (35 ml) were added cyclohexanecarbaldehyde (5.33 g) and sodium cyanoborohydride (3.78 g) under ice-cooling and the mixture was stirred at room temperature. After one hour, the reaction mixture was concentrated and water and saturated brine were added. The mixture was extracted 3 times with ethyl acetate. The organic layers were combined, washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated and the residue was purified by column chromatography (silica gel, hexane/ethyl acetate=15/1) to give 3-chloro-N-cyclohexylmethyl-4-methylaniline as a pale-yellow oil (9.64 g).

Aufarbeitung

  1. temperaturecooling
  2. concentrationthe reaction mixture was concentrated
  3. additionwater and saturated brine were added
  4. extractionThe mixture was extracted 3 times with ethyl acetate
  5. washwashed with saturated brine
  6. dry with materialdried over anhydrous magnesium sulfate
  7. customThe solvent was evaporated
  8. customthe residue was purified by column chromatography (silica gel, hexane/ethyl acetate=15/1)

Quellen und Nachweise

ORD-Eintrag
ord-3e52b5b5d247401188ee0de499d44178
Quelldatensatz
uspto-grants-2003_06
Patentnummer
US06573274B1

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