Methane → HCID 13561832, compound

HRID 414337Notes

Reaction equation

HRID 414337 reaction equation
[C:1]([C:3]([C:20]#[N:21])=[CH:4][NH:5][NH:6][C:7]1[C:12]([Cl:13])=[CH:11][C:10]([S:14][C:15]([F:18])([F:17])[F:16])=[CH:9][C:8]=1[Cl:19])#[N:2].C>C(OCCO)C>[NH2:2][C:1]1[N:6]([C:7]2[C:12]([Cl:13])=[CH:11][C:10]([S:14][C:15]([F:16])([F:17])[F:18])=[CH:9][C:8]=2[Cl:19])[N:5]=[CH:4][C:3]=1[C:20]#[N:21]

Participants

4

Reactant 2

HCID 297MethaneHCID 13561831HCID 13561831, compound

Product 1

HCID 13561832HCID 13561832, compoundYield 70%

Reagents, catalysts & solvents 1

HCID 8076Glycol monoethyl etherSolvent

Procedure

14.1 g (0.04 mole) of 1-(2,2-dicyanethen-1-yl)-2-(2,6-dichloro-4-trifluoromethylthio-phenyl)-hydrazine in 30 ml of ethylene glycol monoethyl ether are heated under reflux for 2 hours. Active charcoal is added to the hot solution, the mixture is filtered and the filtrate is diluted with 60 ml of water. The precipitate which has separated out is filtered off with suction and dried. 9.8 g (70% of theory) of 5-amino-4-cyano-1-(2,6-dichloro-4-trifluoromethylthio-phenyl)-pyrazole of melting point 185° C. to 187° C. are obtained. ##STR121##

Workup

  1. temperatureunder reflux for 2 hours
  2. filtrationthe mixture is filtered
  3. additionthe filtrate is diluted with 60 ml of water
  4. customThe precipitate which has separated out
  5. filtrationis filtered off with suction
  6. customdried

Sources & evidence

ORD record
ord-01c3903b8d644a4d91eb9e2a85e21e58
Source dataset
uspto-grants-1988_12
Patent number
US04791212

Reaction notes

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