Hydrochloric Acid → 3-Hydroxy-5-keto-4-phenylazo-3-cyclohexenecarboxylic acid

HRID 616874Notes

Reaction equation

HRID 616874 reaction equation
[Na].[OH:2][C:3]1[CH2:4][CH:5]([C:10]([OH:12])=[O:11])[CH2:6][C:7](=[O:9])[CH:8]=1.[Cl-].[C:14]1([N+:20]#[N:21])[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1.NC1C=CC=CC=1.Cl.N([O-])=O.[Na+]>O.CO>[OH:2][C:3]1[CH2:4][CH:5]([C:10]([OH:12])=[O:11])[CH2:6][C:7](=[O:9])[C:8]=1[N:21]=[N:20][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1

Participants

9

Procedure

13.8 G. of sodium were dissolved in 900 ml. of methanol. 46.8 G. of 3-hydroxy-5-keto-3-cyclohexenecarboxylic acid were added to this solution. The mixture was stirred, maintained between -4° C. and -8° C. with a cooling bath and treated over a period of 30 minutes with a phenyl diazonium chloride solution prepared from 27.9 g. of aniline, 450 ml. of water, 72 ml. of concentrated hydrochloric acid and 21.0 g. of sodium nitrite in 90 ml. of water. The mixture was stirred -5° C. to -10° C. for an additional hour. The resulting red precipitate was removed by filtration under vacuum and washed with about 1000 ml. of water, thereby there was obtained 3-hydroxy-5-keto-4-phenylazo-3-cyclohexenecarboxylic acid of melting point 218° C.

Workup

  1. temperaturemaintained between -4° C. and -8° C. with a cooling bath
  2. customprepared from 27.9 g
  3. stirringThe mixture was stirred -5° C. to -10° C. for an additional hour
  4. customThe resulting red precipitate was removed by filtration under vacuum
  5. washwashed with about 1000 ml

Sources & evidence

ORD record
ord-d1a9d283acfb44b9bc43ae8e25b18890
Source dataset
uspto-grants-1978_02
Patent number
US04076810

Reaction notes

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