Sodium Acetate → HCID 178460147, compound
Reaction equation
[C:1]([CH:6]1[C:11](=[O:12])[CH2:10][CH:9]([C:13]2[C:18]([CH3:20])([CH3:19])[CH2:17][CH2:16][CH2:15][C:14]=2[CH3:21])[CH2:8][C:7]1=[O:22])(=O)[CH2:2][CH2:3][CH3:4].[Cl-].[CH2:24]([O:27][NH3+:28])[CH:25]=[CH2:26].C([O-])(=O)C.[Na+]>C(O)C>[CH2:24]([O:27][NH:28][C:1](=[C:6]1[C:7](=[O:22])[CH2:8][CH:9]([C:13]2[C:18]([CH3:20])([CH3:19])[CH2:17][CH2:16][CH2:15][C:14]=2[CH3:21])[CH2:10][C:11]1=[O:12])[CH2:2][CH2:3][CH3:4])[CH:25]=[CH2:26]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
8.0 parts by weight of 2-butyryl-5-(1,3,3-trimethylcyclohex-1-en-2-yl)-cyclohexane-1,3-dione are reacted with 2.9 parts by weight of allyloxyammonium chloride and 2.4 parts by weight of sodium acetate in 100 parts by volume of ethanol and the mixture is worked up, by a procedure similar to that of Example 1. 9.0 parts by weight of 2-(1-allyloxyaminobutylidene)-5-(1,3,3-trimethylcyclohex-1-en-2-yl)-cyclohexane-1,3-dione are obtained as a viscous oil (active ingredient No.2).
Sources & evidence
- ORD record
- ord-62e44a79a9b54348a0b7f7a333300f31
- Source dataset
- uspto-grants-1986_02
- Patent number
- US04568383
Reaction notes
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