Reaction #551989

ord-b19edbceb76a45d7978f32107fbaf2d2

Reaction equation

O=CCCOc1ccccc1
3-phenoxypropionaldehyde
[CH3][Mg][I]
methylmagnesium
[CH3][Mg][I]
methylmagnesium iodide
Cl
hydrochloric acid
CC(O)CCOc1ccccc1
4-phenoxy-2-butanol
Yield 67.0%

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Otherby Grignard reaction
  2. 2
    Temperaturewhile maintaining a temperature of not more than 20° C
  3. 3
    Otherthe solution was separated into two phases, which phases
  4. 4
    Otherwere then separated from each other
  5. 5
    WashThe ether layer was washed with an aqueous sodium bicarbonate solution
  6. 6
    Washwashed with water
  7. 7
    Dryingdried with anhydrous sodium sulfate
  8. 8
    Othercondensed under reduced pressure

Procedure

24.9 g of methyl iodide was reacted with 7.26 g of magnesium in 150 ml of anhydrous diethyl ether to obtain methylmagnesium iodide by Grignard reaction. To a solution consisting of 20 g of 3-phenoxypropionaldehyde and 200 ml of anhydrous diethyl ether was added dropwise the methylmagnesium while maintaining a temperature of not more than 20° C. To the reaction solution was added 25 ml of concentrated hydrochloric acid and the solution was separated into two phases, which phases were then separated from each other. The ether layer was washed with an aqueous sodium bicarbonate solution, washed with water, dried with anhydrous sodium sulfate and then condensed under reduced pressure to obtain 15.0 g of 4-phenoxy-2-butanol having a boiling point of 61° C. to 62° C. at 3 mmHg in a yield of 67%.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04549023uspto-grants-1985_10