Hydrochloric Acid → 2-Chloro-4-hydroxybenzaldehyde

HRID 1787730Notes

Reaction equation

HRID 1787730 reaction equation
[H-].C([Al+]CC(C)C)C(C)C.[Cl:11][C:12]1[CH:19]=[C:18]([OH:20])[CH:17]=[CH:16][C:13]=1[C:14]#N.Cl.[O:22]1CCCC1>O>[Cl:11][C:12]1[CH:19]=[C:18]([OH:20])[CH:17]=[CH:16][C:13]=1[CH:14]=[O:22]

Participants

6

Conditions

Temperature
-78 °C

Procedure

Diisobutylaluminium hydride (1M in hexane, 240 mL, 240 mmol) was added to a solution of 2-chloro-4-hydroxybenzonitrile (15 g, 97.7 mmol) in tetrahydrofuran (200 mL), cooled to −78° C., and the mixture was stirred at this temperature for 1 hour then at room temperature for 18 hours. The mixture was then cooled to 0° C. and 1M hydrochloric acid (80 mL) was added dropwise. The reaction mixture was diluted with water (200 mL) and filtered, washing through with ethyl acetate (×2). The layers of the filtrate were separated and the organic solution was dried over magnesium sulfate and concentrated in vacuo. Trituration of the residue with dichloromethane afforded the title compound as a solid in 84% yield, 12.92 g.

Workup

  1. waitat room temperature for 18 hours
  2. temperatureThe mixture was then cooled to 0° C.
  3. filtrationfiltered
  4. washwashing through with ethyl acetate (×2)
  5. customThe layers of the filtrate were separated
  6. dry with materialthe organic solution was dried over magnesium sulfate
  7. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-00ea2eff8b1942c3a6542fb6da338ae6
Source dataset
uspto-grants-2009_03
Patent number
US07511057B2

Reaction notes

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