Hydrochloric Acid → 2-(4-Vinylphenyl)ethanol

HRID 505693Notes

Reaction equation

HRID 505693 reaction equation
[CH2:1]1[O:3][CH2:2]1.Cl.[CH2:5]1[CH2:9]O[CH2:7][CH2:6]1>>[CH:6]([C:5]1[CH:9]=[CH:7][C:6]([CH2:2][CH2:1][OH:3])=[CH:5][CH:9]=1)=[CH2:7]

Participants

4

Conditions

Temperature
0 °C

Procedure

To a VP-MgCl solution as prepared in Example 12 of this section was added a solution of 4.84 g ethylene oxide (0.11 mol) in 50 ml THF. The solution was added via additional funnel over one hour, maintaining the reaction mixture at 0° C. Keep stir at 0° C. for one more hour after the addition was finished. The reaction was then stirred for an additional 1 h at 0° C. 60 ml of 2 M aqueous hydrochloric acid (HCl) solution was added via the addition funnel, maintaining the temperature below 20° C. The reaction was filtered and extracted two times with 100 mL of diethyl ether. The organic phases were combined, dried over MgSO4 and filtered. The diethyl ether was removed by vacuum evaporation at room temperature. 11.2 g white waxy solid, 75.7%). 1H NMR (DMSO-d6): δ 7.20-δ 7.40 (m, 4H, aromatic), δ 6.72 (m, 1H, vinyl), δ 5.75 (d, 1H, vinyl), δ 5.23 (d, 1H, vinyl), δ 4.70 (t, 1H, OH), δ 3.65 (t, 2H, CH2—O), δ 2.72 (t, 2H, CH2—C).

Workup

  1. customTo a VP-MgCl solution as prepared in Example 12 of this section
  2. additionThe solution was added via additional funnel over one hour
  3. additionafter the addition
  4. stirringThe reaction was then stirred for an additional 1 h at 0° C
  5. temperaturemaintaining the temperature below 20° C
  6. filtrationThe reaction was filtered
  7. extractionextracted two times with 100 mL of diethyl ether
  8. dry with materialdried over MgSO4
  9. filtrationfiltered
  10. customThe diethyl ether was removed by vacuum evaporation at room temperature

Sources & evidence

ORD record
ord-1ce946f15acf4b54ad771f8e11d054dd
Source dataset
uspto-grants-2010_08
Patent number
US07781529B2

Reaction notes

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