Zinc Acetate → Zinc

HRID 1701984Notes

Reaction equation

HRID 1701984 reaction equation
[C:1](=O)([O-])[OH:2].[NH4+].C([O-])(=O)C.[Zn+2:10].C([O-])(=O)C.[CH:15]1([C:21]2[CH:26]=[CH:25][C:24]([OH:27])=[CH:23][CH:22]=2)[CH2:20][CH2:19][CH2:18][CH2:17][CH2:16]1.[C:28]1([OH:34])[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1.C=O>>[Zn:10].[CH:15]1([C:21]2[CH:22]=[CH:23][C:24]([OH:27])=[CH:25][CH:26]=2)[CH2:16][CH2:17][CH2:18][CH2:19][CH2:20]1.[C:28]1([OH:34])[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1.[CH2:1]=[O:2]

Participants

5

Reactant 3

HCID 11192Zinc AcetateHCID 14013Ammonium BicarbonateHCID 86738833HCID 86738833, compound

Product 2

HCID 23994ZincHCID 86738833HCID 86738833, compound

Procedure

A powdery mixture of 10 g of ammonium hydrogen carbonate and 13 g of zinc acetate was added portionwise to 100 g of the resulting p-cyclohexylphenol/phenol/formaldehyde co-condensate kept at 170° C. with stirring. There was obtained a pale yellow transparent zinc salt of the p-cyclohexylphenol/phenol/formaldehyde co-condensate.

Workup

  1. customkept at 170° C.

Sources & evidence

ORD record
ord-4918f2e271d14ecf8124d78b78db5f7d
Source dataset
uspto-grants-1983_04
Patent number
US04379897

Reaction notes

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