Ethanol → (Z)-Methyl 3-Methylhepta-2,6-dienoate

HRID 1445376Notes

Reaction equation

HRID 1445376 reaction equation
C[Li].[C:3]([O:11][CH3:12])(=[O:10])[C:4]#[C:5][CH2:6][CH2:7][CH:8]=[CH2:9].[CH2:13](O)C>C1COCC1.CCOCC.[Cu]I>[CH3:13]/[C:5](/[CH2:6][CH2:7][CH:8]=[CH2:9])=[CH:4]/[C:3]([O:11][CH3:12])=[O:10]

Participants

7

Conditions

Temperature
-20 °C

Procedure

A suspension of copper(I) iodide (12.38 g, 65 mmol) in 150 mL of dry THF under a nitrogen atmosphere was cooled to −20° C., and methyllithium (1.6 M in ether, 81.5 mL, 130 mmol) was added dropwise over 15 min. The solution was cooled to −78° C., and 4.49 g (32.5 mmol) of the compound from Example 19 in 15 mL of dry THF was added gradually, keeping the temperature below −70° C. After 1 h, 40 mL of ethanol was added cautiously, and the mixture was allowed to warm to room temperature. The mixture was diluted with ether, and washed with satd aq NH4Cl (200 mL), 5N NH3 (4×250 mL), water (200 mL), and brine (200 mL), dried, and the bulk of the solvent was evaporated to give the title compound (6.8 g, 100%) as an oil. The material had only minor solvent contamination and was adequate for use in the next reaction.

Workup

  1. temperatureThe solution was cooled to −78° C.
  2. customthe temperature below −70° C
  3. temperatureto warm to room temperature
  4. washwashed with satd aq NH4Cl (200 mL), 5N NH3 (4×250 mL), water (200 mL), and brine (200 mL)
  5. customdried
  6. customthe bulk of the solvent was evaporated

Sources & evidence

ORD record
ord-ae35a02afabc4583a3ebdd97ccd7c45c
Source dataset
uspto-grants-2010_02
Patent number
US07666861B2

Reaction notes

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