Benzaldehyde, 5-chloro-2-hydroxy-, oxime → 5-Chloro-2-hydroxybenzonitrile

HRID 1587801Notes

Reaction equation

HRID 1587801 reaction equation
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([OH:11])=[C:6]([CH:10]=1)[CH:7]=[N:8]O>C(OC(=O)C)(=O)C>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([OH:11])=[C:6]([C:7]#[N:8])[CH:10]=1

Participants

3

Conditions

Temperature
4 °C

Procedure

A solution of 5-chloro-2-hydroxybenzaldoxime (4.2 g) in acetic anhydride (15 ml) was heated for 4 hours at reflux, then allowed to stand for 16 hours at ambient temperature. The mixture was added to a vigorously stirred ice-water mixture and after one hour the resulting solid was collected by filtration. 2M Sodium hydroxide solution (120 ml) was added to a stirred solution of this solid in methanol (50 ml) and the mixture stirred for 20 minutes. The pH of the mixture was then adjusted to 4.0 with 2M hydrochloric acid solution. The mixture was cooled to 4° C. and the white precipitate collected by filtration to give 4-chloro-2-cyanophenol (2.6 g), m.p. 166°-168° C.; NMR (CDCl3 /d6 -DMSO): 6.69(1H,d,J=8 Hz), 7.04(1H,dd,J=8,2.5 Hz), 7.11(1H,d,J=2.5 Hz), 10.33(1H,s).

Workup

  1. temperatureat reflux
  2. filtrationwas collected by filtration
  3. addition2M Sodium hydroxide solution (120 ml) was added to a stirred solution of this solid in methanol (50 ml)
  4. filtrationthe white precipitate collected by filtration

Sources & evidence

ORD record
ord-c0d29a52fb914366a9e63cc70e922559
Source dataset
uspto-grants-1993_06
Patent number
US05219874

Reaction notes

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