Valproate → Magnesium Valproate

HRID 1455714

反応式

HRID 1455714 の反応式
[C:1]([O-:10])(=[O:9])[CH:2]([CH2:6][CH2:7][CH3:8])[CH2:3][CH2:4][CH3:5].O.[C:12]([O-:21])(=[O:20])[CH:13]([CH2:17][CH2:18][CH3:19])[CH2:14][CH2:15][CH3:16].[Mg+2:22].C([O-])(=O)C(CCC)CCC>O>[C:1]([O-:10])(=[O:9])[CH:2]([CH2:6][CH2:7][CH3:8])[CH2:3][CH2:4][CH3:5].[Mg+2:22].[C:12]([O-:21])(=[O:20])[CH:13]([CH2:17][CH2:18][CH3:19])[CH2:14][CH2:15][CH3:16]

参加物

4

反応物 2

HCID 3549980ValproateHCID 71439018Magnesium;bis(2-propylpentanoate);hydrate

生成物 1

HCID 147515Magnesium Valproate

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

Surprisingly, the inventors have discovered that a heretofore unknown valproate salt, magnesium valproate hydrate, a white solid having the molecular formula C16H30O4Mg.x H2O, is recovered in high yields from an alcoholic solution of magnesium valproate by adding a polar, non-oxygen-containing organic solvent having a boiling point of about 130° C. or lower in a volume sufficient to reduce the solubility of the magnesium valproate in the resulting reaction mixture to less than about 0.01 g/mL. The polar, non-oxygen-containing organic solvent is acetonitrile, propionitrile, butyronitrile, or isobutyronitrile. Acetonitrile is most preferred.

後処理

  1. customis recovered

出典と根拠

ORDレコード
ord-6aaabd3d5f824156baa1b3cd9b66066c
出典データセット
uspto-grants-2009_01
特許番号
US07482486B2

関連ノート

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