Hydrochloric Acid → HCID 11301002, Verbindung

HRID 1290279Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1290279
[C:1]([C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([C:11]([CH3:14])([CH3:13])[CH3:12])[C:6]=1[OH:15])([CH3:4])([CH3:3])[CH3:2].[C:16]([OH:20])(=[O:19])[CH:17]=O.[ClH:21]>C(O)(=O)C>[C:11]([C:7]1[CH:8]=[C:9]([CH:17]([Cl:21])[C:16]([OH:20])=[O:19])[CH:10]=[C:5]([C:1]([CH3:4])([CH3:3])[CH3:2])[C:6]=1[OH:15])([CH3:14])([CH3:13])[CH3:12]

Komponenten

5

Reaktionsbedingungen

Temperatur
10 °C

Versuchsvorschrift

309.5 g (1.5 Mol) of 2,6-di-tert-butylphenol and 266.5 g (1.8 mol) of 50% aqueous glyoxylic acid are dissolved in 1400 ml of glacial acetic acid. Then, 200 g (5.5 mol) of gazeous hydrogen chloride are introduced into this solution over a period of 2.5 hours under stirring and cooling in an ice bath to keep the temperature in the 10°-25° C. range. The mixture is then stirred at room temperature overnight, cooled to 10° C., the solid is isolated by filtration on a Buechner funnel and washed with 1000 ml water. The slightly yellow and still wet cake of the intermediate product weighs about 565 g.

Aufarbeitung

  1. temperaturecooling in an ice bath
  2. customin the 10°-25° C. range
  3. stirringThe mixture is then stirred at room temperature overnight
  4. customthe solid is isolated by filtration on a Buechner funnel
  5. washwashed with 1000 ml water

Quellen und Nachweise

ORD-Eintrag
ord-fb87e6ba57d8423c8479e793ac7265c2
Quelldatensatz
uspto-grants-1998_05
Patentnummer
US05750765

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