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

HRID 2261232
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HRID 2261232 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 2

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

생성물 1

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

시약·촉매·용매 3

HCID 962Water용매HCID 3776Isopropanol용매HCID 312751,4-Dioxane용매

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-4a99a8c073314835aff1f358171d5cd1
출처 데이터셋
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07846922B2

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