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Lithium Hydroxide → 4-(3-Methyl-1,2,4-oxadiazol-5-yl)benzoic acid

HRID 2261232
ノート
印刷プレビュー

反応式

HRID 2261232 の反応式
[CH3:1][C:2]1[N:6]=[C:5]([C:7]2[CH:16]=[CH:15][C:10]([C:11]([O:13]C)=[O:12])=[CH:9][CH:8]=2)[O:4][N:3]=1.[OH-].[Li+]>O1CCOCC1.O.C(O)(C)C>[CH3:1][C:2]1[N:6]=[C:5]([C:7]2[CH:16]=[CH:15][C:10]([C:11]([OH:13])=[O:12])=[CH:9][CH:8]=2)[O:4][N:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 2

HCID 3939Lithium HydroxideHCID 11096067Methyl 4-(3-methyl-1,2,4-oxadiazol-5-yl)benzoate

生成物 1

HCID 221101114-(3-Methyl-1,2,4-oxadiazol-5-yl)benzoic acid

試薬・触媒・溶媒 3

HCID 962Water溶媒HCID 3776Isopropanol溶媒HCID 312751,4-Dioxane溶媒

実験手順

Methyl 4-(3-methyl-1,2,4-oxadiazol-5-yl)benzoate (J. R. Young and R. J. DeVita, Tetrahedron Lett., 1998, 39, 3931) was dissolved in a mixture of dioxan (110 ml), water (70 ml) and isopropanol (30 ml), and lithium hydroxide (1.38 g) was added. The mixture was stirred at room temperature for ca 5 h and then the mixture was acidified to ca pH 4 by addition of Amberlyst 15 H+ resin. The resin was removed by filtration and the filtrate was concentrated in vacuo. The solid white precipitate which was obtained was collected by filtration, washed with water on the filter and dried in vacuo at 40° C. for 48 h to give the title compound (D18) (4.23 g).

後処理

  1. additionwas added
  2. additionby addition of Amberlyst 15 H+ resin
  3. customThe resin was removed by filtration
  4. concentrationthe filtrate was concentrated in vacuo
  5. customThe solid white precipitate which was obtained
  6. filtrationwas collected by filtration
  7. washwashed with water on the
  8. filtrationfilter
  9. customdried in vacuo at 40° C. for 48 h

出典と根拠

ORDレコード
ord-4a99a8c073314835aff1f358171d5cd1
出典データセット
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07846922B2

反応ノート

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