Potassium Hydroxide → HCID 178443359, compound
Reaction equation
[C-:1]1([C:6]([CH:8]([CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH3:22])[C:9]([O:11]CC)=[O:10])=[O:7])[CH:5]=[CH:4][CH:3]=[CH:2]1.[CH-:23]1[CH:27]=[CH:26][CH:25]=[CH:24]1.[Fe+2:28].[OH-].[K+]>C(O)C>[C-:1]1([C:6]([CH:8]([CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH3:22])[C:9]([OH:11])=[O:10])=[O:7])[CH:2]=[CH:3][CH:4]=[CH:5]1.[CH-:23]1[CH:27]=[CH:26][CH:25]=[CH:24]1.[Fe+2:28]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
An amount of 12.4 g of ethyl ferrocenoylundecanate prepared in (1) above and 2.9 g of potassium hydroxide were refluxed for 2 hours in an ethanol solvent and then was subjected to acid treatment to obtain 11.3 g of ferrocenoylundecanic acid represented by the following formula: ##STR27##
Sources & evidence
- ORD record
- ord-676d18241f724c27a1a3db121f208fe1
- Source dataset
- uspto-grants-1992_01
- Patent number
- US05082539
Reaction notes
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