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Sodium Hydroxide → 1,5-Diethyl-1H-pyrazole-3-carboxylic acid

HRID 1825341
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HRID 1825341 반응식
[CH2:1]([N:3]1[C:7]([CH2:8][CH3:9])=[CH:6][C:5]([C:10]([O:12]CC)=[O:11])=[N:4]1)[CH3:2].[OH-].[Na+].C(OCC)(=O)C.O>C(O)C>[CH2:1]([N:3]1[C:7]([CH2:8][CH3:9])=[CH:6][C:5]([C:10]([OH:12])=[O:11])=[N:4]1)[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 14798Sodium Hydroxide2회HCID 22145420Ethyl 1,5-diethylpyrazole-3-carboxylateHCID 22728543Water ethylacetate

생성물 1

HCID 221453751,5-Diethyl-1H-pyrazole-3-carboxylic acid수율 82.8%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

Ethyl 1,5-diethylpyrazole-3-carboxylate (20.7 g) in ethanol (250 ml) was treated with 2.5M aqueous NaOH (50.6 ml), and the mixture was stirred overnight. A further 4.2 ml of 2.5M NaOH was then added and stirring continued for a further 1 hour. The mixture was then poured into ethyl acetate/water. The mixture was shaken vigorously and the aqueous phase removed. The pH of the aqueous phase was adjusted to 2.0 using 1M aqueous HCl and saturated with NaCl. The aqueous layer was then extracted with 20% toluene/80% THF (5×100 ml). The combined organic extracts were dried over MgSO4 and evaporated in vacuo. The residue was triturated with hexane/diethyl ether to give the acid as a solid (14.69 g); υmax(CH2Cl2) 3450, 2750, 2596, 1697, cm−1; δ(CDCl3) 1.31 (3H, t, J 7 Hz), 1.44 (3H, t,J 7 Hz) 2.64 (2H, q, J 7 Hz), 4.20 (2H, q, J 7 Hz), 6.64 (1H,s) ppm.

후처리

  1. stirringstirring
  2. waitcontinued for a further 1 hour
  3. stirringThe mixture was shaken vigorously
  4. customthe aqueous phase removed
  5. extractionThe aqueous layer was then extracted with 20% toluene/80% THF (5×100 ml)
  6. dry with materialThe combined organic extracts were dried over MgSO4
  7. customevaporated in vacuo
  8. customThe residue was triturated with hexane/diethyl ether

출처 및 근거

ORD 기록
ord-b95e053a23db4b2ba3920b7037546073
출처 데이터셋
uspto-grants-2006_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07045619B2

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