Carbon Tetrachloride → HCID 20370622, compound

HRID 615977Notes

Reaction equation

HRID 615977 reaction equation
[CH3:1][N:2]([CH3:19])[C:3](=[O:18])[CH:4]([CH3:17])[N:5]1[C:9](C)=C[C:7]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[N:6]1.ClO[C:22](C)(C)C.BrBr.[C:28]([Cl:32])(Cl)(Cl)Cl>C(O)(=O)C>[Cl:32][C:28]1[C:7]([C:11]2[CH:12]=[CH:13][CH:14]=[CH:15][C:16]=2[CH3:22])=[N:6][N:5]([CH:4]([CH3:17])[C:3]([N:2]([CH3:1])[CH3:19])=[O:18])[CH:9]=1

Participants

6

Reactant 4

HCID 5943Carbon TetrachlorideHCID 24408BromineHCID 521297Tert-Butyl hypochloriteHCID 20370380N,N-Dimethyl-2-(5-methyl-3-phenyl-1H-pyrazol-1-yl)propanamide

Product 1

HCID 20370622HCID 20370622, compound

Reagents, catalysts & solvents 1

HCID 176Acetic AcidSolvent

Procedure

Following the procedure of Example 108, but substituting N,N,α-trimethyl-3-(o-tolyl)pyrazole-1-acetamide for N,N,α,5-tetramethyl-3-phenylpyrazole-1-acetamide, tert-butyl hypochlorite for bromine, and carbon tetrachloride for acetic acid as the reaction solvent, there was obtained 4-chloro-N,N,α-trimethyl-3-(o-tolyl)pyrazole-1-acetamide having a melting point of 69°-71.5° C.

Sources & evidence

ORD record
ord-ce9e75cdcee745dbb32db6898a5450d2
Source dataset
uspto-grants-1978_02
Patent number
US04072498

Reaction notes

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