Hexane → 2,3-Dimethyl-1-butene

HRID 2049500

Reaction equation

HRID 2049500 reaction equation
[CH2:1]=[CH:2][CH3:3].[CH3:4][CH2:5][CH2:6][CH2:7][CH2:8][CH3:9]>>[CH3:1][C:2]([CH:5]([CH3:6])[CH3:4])=[CH2:3].[CH3:1][C:8]([CH2:7][CH2:6][CH3:5])=[CH2:9]

Participants

4

Conditions

Temperature
32 °C

Procedure

Ta(C5Me5)(propylene)Cl2 (0.11 g, 0.25 mmol) was dissolved in 2.5 ml of hexane in a 20 ml glass pressure bottle containing a small teflon-coated magnetic stir bar. A pressure head equipped with a rubber system for sampling the mixture was clamped to the glass vessel and the vessel was pressurized to 40 psi with propylene and immersed in a stirred bath maintained at 32° C. Samples were withdrawn by syringe at regular intervals, quenched with gaseous oxygen, and analyzed by gas chromatography. 2,3-dimethyl-1-butene and 2-methyl-1-pentene formed steadily in a 98:2 ratio at a rate of 0.0014 M min-1 or k1 =0.014 min-1 since the catalyst concentration is 0.1 M. At 40° k1 =0.039 min-1 which amounts to about 1 turnover per hour per Ta. The rate increases markedly at higher temperatures (ΔH++ =19±1 kcal mol-1, ΔS ++ =14±3 eu).

Workup

  1. additioncontaining a small teflon-coated magnetic stir bar
  2. customA pressure head equipped with a rubber system
  3. aliquotfor sampling the mixture
  4. customimmersed in a stirred bath
  5. customSamples were withdrawn by syringe at regular intervals
  6. customquenched with gaseous oxygen

Sources & evidence

ORD record
ord-413e7c60ffc64e2bb09880c9c9e25da1
Source dataset
uspto-grants-1980_04
Patent number
US04197419

Linked notes

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