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Ammonium Hydroxide → HCID 66958295, 화합물

HRID 1984368
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HRID 1984368 반응식
[CH2:1]([N:8]1[C:12]([CH3:13])=[CH:11][C:10]([C:14]([O:16]CC)=O)=[N:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[OH-].[NH4+:20]>CO>[CH2:1]([N:8]1[C:12]([CH3:13])=[CH:11][C:10]([C:14]([NH2:20])=[O:16])=[N:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14923Ammonium HydroxideHCID 2755348ethyl 1-benzyl-5-methyl-1H-pyrazole-3-carboxylate

생성물 1

HCID 66958295HCID 66958295, 화합물

시약·촉매·용매 1

HCID 887Methanol용매

반응 조건

온도
125 °C

실험 절차

A mixture of ethyl 1-benzyl-5-methyl-1H-pyrazole-3-carboxylate (57.57 g, 0.236 mol), concentrated ammonium hydroxide (114 mL), and methanol (114 mL) was heated at 125° C. for 39 hours in a pressure vessel. After cooling to ambient temperature, the vessel was placed in an ice bath and the reaction solution was stirred for 30 minutes until a precipitate formed. The precipitate was isolated by filtration and washed with water to yield 28.22 g of 1-benzyl-5-methyl-1H-pyrazole-3-carboxamide.

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

후처리

  1. temperatureAfter cooling to ambient temperature
  2. customthe vessel was placed in an ice bath
  3. customformed
  4. customThe precipitate was isolated by filtration
  5. washwashed with water

출처 및 근거

ORD 기록
ord-99faaf667b254a33ba88ceae1cf95593
출처 데이터셋
uspto-grants-2009_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07544697B2

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