Isobutylene → 1-tert-Butyl-4-(3-chloro-2-methylpropyl)benzene

HRID 1065179

Reaktionsgleichung

Reaktionsgleichung von HRID 1065179
[CH2:1]=[C:2]([CH3:4])[CH3:3].[CH3:5][CH:6]([CH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)[CH2:7][Cl:8].F>>[CH3:5][CH:6]([CH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)[CH2:7][Cl:8].[CH3:5][CH:6]([CH2:9][C:10]1[CH:15]=[CH:14][C:13]([C:2]([CH3:4])([CH3:3])[CH3:1])=[CH:12][CH:11]=1)[CH2:7][Cl:8]

Komponenten

5

Versuchsvorschrift

20 parts by weight of isobutene are passed into a mixture of 68 parts by weight of 2-methyl-3-phenylpropyl chloride and 3 parts by weight of hydrogen fluoride at 0° C. The mixture is then stirred for 12 hours at room temperature. The crude product is washed with water, dried over Na2CO3 and distilled. 36 parts by weight of 2-methyl-3-phenylpropyl chloride, boiling point 105° C./16 mm Hg and 32 parts by weight of 2-methyl-3-(p-tert.-butylphenyl)-propyl chloride, boiling point 80° C.-81° C./0.02 mm Hg, are obtained.

Aufarbeitung

  1. washThe crude product is washed with water
  2. dry with materialdried over Na2CO3
  3. distillationdistilled

Quellen und Nachweise

ORD-Eintrag
ord-5821a7df913a4bd5b7c6ff5bdf662702
Quelldatensatz
uspto-grants-1982_05
Patentnummer
US04328380

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