Reaktion #2146732

ord-7207d305630b4f39bd3f7fcce846f8b4

Reaktionsgleichung

CC(C)CC1=CCCCC1
1-isobutylcyclohex-1-ene
[Cl][Sn]([Cl])([Cl])[Cl]
tin tetrachloride
C/C=C/C(=O)Cl
crotonyl chloride
C/C=C/C(=O)C1CCCC=C1CC(C)C
(E)-1-(2-isobutylcyclohex-2-enyl)but-2-en-1-one
Ausbeute 30.2%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.STIRRINGThe resulting mixture was stirred for 1 h at −70° C.
  2. 2
    Waschenphase was first washed with concentrated NaOH
  3. 3
    Trocknenwith H2O, dried (MgSO4)
  4. 4
    Sonstigethe solvent evaporated
  5. 5
    workup.DISTILLATIONShort-path Vigreux-distillation (0.15 mbar, bath temperature: 160° C.) of the crude product (592 g)
  6. 6
    Sonstigegave a fraction (495 g, boiling range: 90-130° C.) that
  7. 7
    workup.DISTILLATIONwas redistilled
  8. 8
    Sonstigea short-path Vigreux-column (0.11 mbar, bath temperature: 160° C.)

Vorschrift

At −70° C., a solution of tin tetrachloride (533 ml, 4.54 mol, 1.4 eq.) in dichloromethane (2.5 l) was treated with crotonyl chloride (350 ml, 90%, 3.24 mol, 1.0 eq.). The resulting solution was stirred for 30 min. and treated within 1.5 h with a solution of 1-isobutylcyclohex-1-ene (448 g, 3.24 mol) in dichloromethane (400 ml). The resulting mixture was stirred for 1 h at −70° C. and poured into ice/H2O. The org. phase was first washed with concentrated NaOH then with H2O, dried (MgSO4), and the solvent evaporated. Short-path Vigreux-distillation (0.15 mbar, bath temperature: 160° C.) of the crude product (592 g) gave a fraction (495 g, boiling range: 90-130° C.) that was redistilled using again a short-path Vigreux-column (0.11 mbar, bath temperature: 160° C.) to give (E)-1-(2-isobutylcyclohex-2-enyl)but-2-en-1-one (202 g, 30%). Boiling point: 120° C. (0.11 mbar).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08278230B2uspto-grants-2012_10