Sodium Acetate → HCID 178460147, compound

HRID 1589100Notes

Reaction equation

HRID 1589100 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

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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