Water → HCID 21418271, compound

HRID 441856Notes

Reaction equation

HRID 441856 reaction equation
[Cl:1][C:2]1[N:6]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)[N:5]=[C:4]([C:13]2[CH:18]=[CH:17][C:16]([Cl:19])=[CH:15][CH:14]=2)[C:3]=1[CH2:20][C:21](N)=[O:22].N([O-])=[O:25].[Na+].O>S(=O)(=O)(O)O>[Cl:1][C:2]1[N:6]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)[N:5]=[C:4]([C:13]2[CH:18]=[CH:17][C:16]([Cl:19])=[CH:15][CH:14]=2)[C:3]=1[CH2:20][C:21]([OH:22])=[O:25]

Participants

5

Procedure

3.5 g of 5-chloro-3-p-chlorophenyl-1-phenyl-pyrazole-4-acetamide are dissolved in 15 ml of 90 % sulfuric acid and while stirring at 20° to 30° a solution of 0.7 g sodium nitrite in a little water is passed dropwise under the surface. Gentle heating is carried out until the evolution of gas is terminated and the mixture is then poured on to an ice and water mixture. 5-Chloro-3-p-chlorophenyl-1-phenylpyrazole-4-acetic acid is produced; F 179.5°-181°.

Workup

  1. temperatureGentle heating
  2. customis terminated
  3. additionthe mixture is then poured on to an ice and water mixture

Sources & evidence

ORD record
ord-d6ddfdac0e7a4dfda2c39de0cd20209c
Source dataset
uspto-grants-1977_08
Patent number
US04042702

Reaction notes

Loading…