2-Ethylhexanoic Acid → Lanthanum

HRID 1460139

Reaction equation

C([O-])(=O)C.[La+3:5].C([O-])(=O)C.C([O-])(=O)C.[CH2:14]([CH:16]([CH2:20][CH2:21][CH2:22][CH3:23])[C:17]([OH:19])=[O:18])[CH3:15]>>[La:5].[CH2:14]([CH:16]([CH2:20][CH2:21][CH2:22][CH3:23])[C:17]([O-:19])=[O:18])[CH3:15].[La+3:5].[CH2:14]([CH:16]([CH2:20][CH2:21][CH2:22][CH3:23])[C:17]([O-:19])=[O:18])[CH3:15].[CH2:14]([CH:16]([CH2:20][CH2:21][CH2:22][CH3:23])[C:17]([O-:19])=[O:18])[CH3:15]

Participants

Reactant 2

HCID 86972-Ethylhexanoic Acid

HCID 13511Lanthanum acetate

Product 2

HCID 23926Lanthanum

HCID 171899Hexanoic acid, 2-ethyl-, lanthanum(3+) salt (3:1)

Procedure

A lanthanum precursor composition was prepared by transcarboxylating 2 grams of lanthanum acetate (40.5% by wt. La) with 8 grams of 2-ethylhexanoic acid to produce lanthanum 2 -ethylhexanoate.

Sources & evidence

ORD record: ord-992c8bb55bdc402c9228d885f7e08dbf
Source dataset: uspto-grants-1991_12
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05070072

Linked notes

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