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

HRID 1655079Notes

Reaction equation

HRID 1655079 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-ae9bd920dec845dd9f1e0e6c5a1b078b
Source dataset
uspto-grants-1995_04
Patent number
US05410064

Reaction notes

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