2,6-Diisopropylnaphthalene → 1-(1-Methylethyl)naphthalene

HRID 1709800Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1709800
C(C1C=CC2C(=CC=C(C(C)C)C=2)C=1)(C)C.C([C:20]1[C:21](C(C)C)=[C:22]([CH:30]([CH3:32])[CH3:31])[C:23]2[C:28]([CH:29]=1)=[CH:27][CH:26]=[CH:25][CH:24]=2)(C)C>>[CH:30]([C:22]1[C:23]2[C:28](=[CH:27][CH:26]=[CH:25][CH:24]=2)[CH:29]=[CH:20][CH:21]=1)([CH3:32])[CH3:31]

Komponenten

3

Versuchsvorschrift

A process for the production of 2,6-diisopropylnaphthalene is disclosed wherein an isopropylation reaction mixture containing isopropylated naphthalenes is subjected to transalkylation with a triisopropylnaphthalene-containing mixture to obtain a mixture containing mono-, di- and tri-isopropylnaphthalenes which is then separated into a first fraction containing monisopropylnaphthalenes, a second fraction containing diisopropylnaphthalenes and a third fraction containing triisopropylnaphthalenes. The first and third fractions are recycled to the above system, while the second fraction is subjected to separation treatments for the recovery of 2,6-diisopropylnaphthalene. The second fraction from which 2,6-diisopropylnaphthalene has been removed is subjected to transalkylation with naphthalene to obtain a monoisopropylnaphthalene-rich mixture which is to be fed to the isopropylation step.

Aufarbeitung

  1. additioncontaining mixture
  2. customto obtain a mixture
  3. customis then separated into a first fraction
  4. additioncontaining monisopropylnaphthalenes
  5. additiona second fraction containing diisopropylnaphthalenes
  6. additiona third fraction containing triisopropylnaphthalenes
  7. customis subjected to separation treatments for the recovery of 2,6-diisopropylnaphthalene
  8. customThe second fraction from which 2,6-diisopropylnaphthalene has been removed

Quellen und Nachweise

ORD-Eintrag
ord-f0b63e10213e485aadb0ef3306afca46
Quelldatensatz
uspto-grants-1990_08
Patentnummer
US04950824

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