Water → HCID 86675565, compound

HRID 2405667Notes

Reaction equation

HRID 2405667 reaction equation
[CH2:1]([C:4](=[CH:8][CH2:9][CH:10]([CH3:12])[CH3:11])[C:5](=[O:7])[CH3:6])[CH:2]=[CH2:3].[H-].[H-].[H-].[H-].[Li+].[Al+3].O.[OH-].[Na+]>C1COCC1>[CH2:1]([CH:4]([CH2:8][CH:9]=[C:10]([CH3:11])[CH3:12])[CH:5]([OH:7])[CH3:6])[CH:2]=[CH2:3]

Participants

6

Conditions

Temperature
-15 °C

Procedure

3-allyl-6-methylheptenone (20.0 g, 120 mmol) was dissolved in anhydrous THF (100 ml) and the solution cooled to −15° C. under stirring. A 3.5M solution of LiAlH4 (in THF/toluene, 12.0 ml, 42 mmol, 0.35 mol. eq.) was added dropwise under argon over 30 min. The reaction mixture was then stirred at −15° C. for 1 hour. The temperature was raised to 0° C., and the mixture carefully hydrolyzed by successive dropwise additions of water (1.60 g), 15% aqueous NaOH (1.60 g) and water (4.80 g), while keeping the reaction mixture at 0° C. The mixture was allowed to warm to room temperature, and the precipitate filtered. Evaporation of the solvent afforded the crude product. Fractional distillation though a 10 cm Vigreux column afforded the desired compound (16.94 g (83% yield).

Workup

  1. stirringThe reaction mixture was then stirred at −15° C. for 1 hour
  2. temperatureThe temperature was raised to 0° C.
  3. customat 0° C
  4. temperatureto warm to room temperature
  5. filtrationthe precipitate filtered
  6. customEvaporation of the solvent
  7. customafforded the crude product
  8. distillationFractional distillation though a 10 cm Vigreux column

Sources & evidence

ORD record
ord-5e2129c29ac44712a7d4a2bb6e134dad
Source dataset
uspto-grants-2014_08
Patent number
US08809256B2

Reaction notes

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