2-Phenoxybenzhydrazide → HCID 53690311, compound

HRID 1493689Notes

Reaction equation

HRID 1493689 reaction equation
[N:1]1[CH:6]=[CH:5][C:4]([C:7]([CH2:9][CH:10]([CH3:12])[CH3:11])=O)=[CH:3][CH:2]=1.[O:13]([C:20]1[CH:29]=[CH:28][CH:27]=[CH:26][C:21]=1[C:22]([NH:24][NH2:25])=[O:23])[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1>C(O)(=O)C>[CH3:11][CH:10]([CH3:12])[CH2:9][C:7](=[N:25][NH:24][C:22](=[O:23])[C:21]1[CH:26]=[CH:27][CH:28]=[CH:29][C:20]=1[O:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)[C:4]1[CH:5]=[CH:6][N:1]=[CH:2][CH:3]=1

Participants

4

Reactant 2

HCID 1426502-PhenoxybenzhydrazideHCID 147428523-methyl-1-(pyridin-4-yl)butan-1-one

Product 1

HCID 53690311HCID 53690311, compound

Reagents, catalysts & solvents 1

HCID 176Acetic AcidCatalyst

Procedure

Following the general method of procedure 4 and making noncritical variations, except 12 drops of glacial acetic acid is added as a catalyst, 9.00 gm (0.055 mole) of isobutyl 4-pyridyl ketone and 12.59 gm (0.055 mole) of 2-phenoxybenzhydrazide yield 13.89 gm (67%) of the title compound having a melting point of 137.6° C.

Sources & evidence

ORD record
ord-5a55bcaeb59d42a4862eff2c5f892475
Source dataset
uspto-grants-1991_06
Patent number
US05023334

Reaction notes

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