Pyridine → N-[(5-tert-Butyl-2-hydroxyphenyl)methyl]acetamide

HRID 364896

Reaktionsgleichung

Reaktionsgleichung von HRID 364896
Cl.[NH2:2][CH2:3][C:4]1[CH:9]=[C:8]([C:10]([CH3:13])([CH3:12])[CH3:11])[CH:7]=[CH:6][C:5]=1[OH:14].N1C=CC=CC=1.[C:21](Cl)(=[O:23])[CH3:22]>O1CCOCC1>[C:21]([NH:2][CH2:3][C:4]1[CH:9]=[C:8]([C:10]([CH3:11])([CH3:13])[CH3:12])[CH:7]=[CH:6][C:5]=1[OH:14])(=[O:23])[CH3:22]

Komponenten

5

Edukt 3

HCID 1049PyridineHCID 6367Acetyl chlorideHCID 212969502-(Aminomethyl)-4-tert-butylphenol hydrochloride

Produkt 1

HCID 13210348N-[(5-tert-Butyl-2-hydroxyphenyl)methyl]acetamide

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 312751,4-DioxaneLösungsmittel

Versuchsvorschrift

43 g (0.2 mole) of 2-aminomethyl-4-(1,1-dimethylethyl)-phenol hydrochloride are suspended in 400 ml of 1,4-dioxane, and 40 ml of pyridine are added. 40 ml (0.55 mole) of acetyl chloride are added dropwise while stirring and cooling with ice. The mixture is then stirred for 2.5 hours at 90° and poured into ice water, and the precipitate which has crystallized out is filtered off with suction.

Aufarbeitung

  1. temperaturecooling with ice
  2. stirringThe mixture is then stirred for 2.5 hours at 90°
  3. customthe precipitate which has crystallized out
  4. filtrationis filtered off with suction

Quellen und Nachweise

ORD-Eintrag
ord-dcd443eda4674388a7bbb90b3deda725
Quelldatensatz
uspto-grants-1986_08
Patentnummer
US04607030

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