Potassium Hydroxide → HCID 178525459, compound
Reaction equation
C([O:6][C:7]([C:9]1[CH:10]=[CH:11][C-:12](C)[CH:13]=1)=[O:8])(=O)CCC.[CH-:15]1[CH:19]=[CH:18][CH:17]=[CH:16]1.[Fe+2:20].[OH-:21].[K+]>C(O)C>[C-:15]1([C:12]([CH2:11][CH2:10][CH2:9][C:7]([OH:6])=[O:8])=[O:21])[CH:19]=[CH:18][CH:17]=[CH:16]1.[CH-:9]1[CH:10]=[CH:11][CH:12]=[CH:13]1.[Fe+2:20]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
An amount of 25.8 g of methyl-4-ferrocenoyl butyrate prepared according to the method of Preparation Example 1 (1) was reacted in ethanol with 11.5 g of potassium hydroxide, to obtain 24.0 g of 4-ferrocenoyl butyric acid represented by the following formula: ##STR58##
Sources & evidence
- ORD record
- ord-1c619e3f93dd4514bfdd9d3c63373380
- Source dataset
- uspto-grants-1992_08
- Patent number
- US05135619
Reaction notes
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