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

HRID 452876
ノート
印刷プレビュー

反応式

HRID 452876 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-b6ed52d5640e4f99bdd536a73b3e5f50
出典データセット
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08492375B2

反応ノート

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