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Ethyl(4,5,6,7,8,8-hexachloro-3a,4,7,7a-tetrahydro-4,7-methano-1H-isoindole-1,3(2H)-dionato-kappaN2)mercury → Phenylmercuric Acetate

HRID 616385
Notes
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Reaction equation

HRID 616385 reaction equation
CC[Hg]N1C(=O)C2C3(Cl)C(Cl)(Cl)C(Cl)(C2C1=O)C(Cl)=C3Cl.C[CH:23](O)[C:24]([O-:26])=[O:25].CC(O)C([O-])=O.[CH:34]1[CH:39]=[CH:38][C:37]([Hg+:40])=[CH:36][CH:35]=1.C([NH3+])CO.N#CN.[Ca]>[Ni]>[CH3:23][C:24]([O:26][Hg:40][C:37]1[CH:38]=[CH:39][CH:34]=[CH:35][CH:36]=1)=[O:25]
ParticipantsProcedureSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 17437Ethyl(4,5,6,7,8,8-hexachloro-3a,4,7,7a-tetrahydro-4,7-methano-1H-isoindole-1,3(2H)-dionato-kappaN2)mercuryHCID 18435199Mercurate(1-), (2-aminoethanolato-N,O)(2-hydroxypropanoato-O1,O2)phenyl-, hydrogenHCID 45051688CID 45051688

Product 1

HCID 16682730Phenylmercuric Acetate

Reagents, catalysts & solvents 1

HCID 935NickelCatalyst

Procedure

N-ethylmercuri-1,2,3,6tetrahydro-3,6-endomethano-3,4,5,6,7,7-hexachlorophthalimide, phenylmercuric monoethanolammonium lactate, nickel-containing compounds and calcium cyanamide.

Sources & evidence

ORD record
ord-749407a433314796ab8124a68961e2ff
Source dataset
uspto-grants-1978_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04073921

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes