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Diisobutylaluminum hydride → (1,3-dimethyl-1H-pyrazol-4-yl)methanol

HRID 2111906
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HRID 2111906 반응식
C([O:3][C:4]([C:6]1[C:7]([CH3:12])=[N:8][N:9]([CH3:11])[CH:10]=1)=O)C.CC(C[AlH]CC(C)C)C>O1CCCC1>[CH3:11][N:9]1[CH:10]=[C:6]([CH2:4][OH:3])[C:7]([CH3:12])=[N:8]1
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4

반응물 2

HCID 14487Diisobutylaluminum hydrideHCID 10313289ethyl 1,3-dimethyl-1H-pyrazole-4-carboxylate

생성물 1

HCID 949772(1,3-dimethyl-1H-pyrazol-4-yl)methanol수율 100%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
0 °C

실험 절차

To a cooled solution (0° C.) of 1,3-dimethyl-1H-pyrazole-4-carboxylic acid ethyl ester (5.0 g, 29.7 mmol) in anhydrous tetrahydrofuran (1000 ml), is added a solution of DIBAL-H (95.1 ml, 95.1 mmol). The reaction mixture is stirred at 0° C. for 2 hours and then quenched with saturated aqueous sodium potassium tartrate and stirred for 2 hours. The layers are separated and the aqueous layer is extracted with ethyl acetate. The combined organic extracts are dried over anhydrous Na2SO4, filtered, and concentrated in vacuo to give 1,3-dimethyl-1H-pyrazol-4-methanol (3.7 g, 100%) which is used without purification. 1H NMR (CDCl3): δ=7.22 (1H, s), 4.46 (2H, s), 3.74 (3H, s), 2.20 (3H, s).

후처리

  1. customquenched with saturated aqueous sodium potassium tartrate
  2. stirringstirred for 2 hours
  3. customThe layers are separated
  4. extractionthe aqueous layer is extracted with ethyl acetate
  5. dry with materialThe combined organic extracts are dried over anhydrous Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-06fc9185d0f1490684127883d0e49999
출처 데이터셋
uspto-grants-2009_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07521462B2

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