Valproic Acid → Magnesium;bis(2-propylpentanoate);hydrate

HRID 1455716

반응식

HRID 1455716 반응식
C(O)(=[O:9])C(CCC)CCC.[O-]CC.[Mg+2:14].[O-]CC.C(#N)C.[C:21]([O-:30])(=[O:29])[CH:22]([CH2:26][CH2:27][CH3:28])[CH2:23][CH2:24][CH3:25].[Mg+2].[C:32]([O-:41])(=[O:40])[CH:33]([CH2:37][CH2:38][CH3:39])[CH2:34][CH2:35][CH3:36]>C(O)C>[OH2:9].[C:21]([O-:30])(=[O:29])[CH:22]([CH2:26][CH2:27][CH3:28])[CH2:23][CH2:24][CH3:25].[Mg+2:14].[C:32]([O-:41])(=[O:40])[CH:33]([CH2:37][CH2:38][CH3:39])[CH2:34][CH2:35][CH3:36]

참가 물질

6

반응물 4

HCID 3121Valproic AcidHCID 6342AcetonitrileHCID 147515Magnesium Valproate2회HCID 164963Magnesium ethanolate

생성물 1

HCID 71439018Magnesium;bis(2-propylpentanoate);hydrate수율 89%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A solution of magnesium valproate in absolute ethanol was obtained in the following manner. To a magnetically stirred, clear, colorless solution of valproic acid (3.17 g; 0.022 mol; Sigma Aldrich Chemical Co.) in 25 mL of absolute ethanol was added 1.14 g (0.01 mol) of magnesium ethoxide solid; residual solid was rinsed in with 1 mL of absolute ethanol. Within 60 minutes, a clear, pale yellow solution was obtained; no heating was observed. One milliliter portions of the solution were aliquoted into test tubes, and a second solvent or solution was added in portions. The results of the additions are summarized in Table 2. A 15 mL portion of acetonitrile was added to an equal volume of the ethanol solution of magnesium valproate. A white precipitate formed, which was isolated by filtration, washed with a fresh portion of acetonitrile, and dried to constant mass. The product, magnesium valproate hydrate, was obtained in 89% yield as a white solid, which exhibited an elemental composition identical to that calculated for magnesium valproate hydrate. The product did not melt at temperatures as high as 300° C. The product was not hygroscopic or deliquescent. The theoretical valproate content (weight %) of magnesium valproate hydrate is 88.6%; the valproate content found by HPLC analysis was 88.5%.

후처리

  1. washresidual solid was rinsed in with 1 mL of absolute ethanol
  2. customa clear, pale yellow solution was obtained
  3. additiona second solvent or solution was added in portions
  4. customThe results of the additions
  5. customA white precipitate formed
  6. customwhich was isolated by filtration
  7. washwashed with a fresh portion of acetonitrile
  8. customdried to constant mass

출처 및 근거

ORD 기록
ord-1ab82aecf7954e3ca2b144c62e98da87
출처 데이터셋
uspto-grants-2009_01
특허 번호
US07482486B2

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