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Formaldehyde → 4-bromo-3-t-butyl-1H-pyrazole-1-ylmethanol

HRID 1983011
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HRID 1983011 반응식
[Br:1][C:2]1[C:3]([C:7]([CH3:10])([CH3:9])[CH3:8])=[N:4][NH:5][CH:6]=1.[CH2:11]=[O:12]>C(N(CC)CC)C.CC(C)=O>[Br:1][C:2]1[C:3]([C:7]([CH3:10])([CH3:9])[CH3:8])=[N:4][N:5]([CH2:11][OH:12])[CH:6]=1
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참가 물질

5

반응물 2

HCID 712FormaldehydeHCID 178441971HCID 178441971, 화합물

생성물 1

HCID 231491454-bromo-3-t-butyl-1H-pyrazole-1-ylmethanol수율 105.2%

시약·촉매·용매 2

HCID 8471Triethylamine촉매HCID 180Acetone용매

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온도
130 °C

실험 절차

The mixture of 3.14 g of 4-bromo-3-t-butyl-1H-pyrazole, 0.93 g of paraformaldehyde and 0.11 g of triethylamine was stirred at 130° C. for 7 hours. After the reaction mixture was cooled to room temperature, acetone was added to the reaction mixture. The mixture was filtered. Hexane was added to the residue obtained by concentration of the filtrate under reduced pressure, as a result, a crystal was formed. The crystal was collected to obtain 3.79 g of 4-bromo-3-t-butyl-1H-pyrazole-1-ylmethanol.

후처리

  1. temperatureAfter the reaction mixture was cooled to room temperature
  2. filtrationThe mixture was filtered
  3. additionHexane was added to the residue
  4. customobtained by concentration of the filtrate under reduced pressure, as a result
  5. customa crystal was formed
  6. customThe crystal was collected

출처 및 근거

ORD 기록
ord-db0ca102a1c24264b3da0eab9fcbad8a
출처 데이터셋
uspto-grants-2009_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07541374B2

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