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Potassium Hydroxide → HCID 178493560, 화합물

HRID 743980
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HRID 743980 반응식
[CH3:1][O:2][C:3]1[CH:8]=[C:7]([O:9][CH3:10])[N:6]=[C:5]([SH:11])[N:4]=1.[OH-].[K+].[N+]([N:17]1[CH:21]=[C:20]([N+:22]([O-:24])=[O:23])[C:19]([CH3:25])=[N:18]1)([O-])=O>O.C(O)C>[CH3:10][O:9][C:7]1[CH:8]=[C:3]([O:2][CH3:1])[N:4]=[C:5]([S:11][C:21]2[NH:17][N:18]=[C:19]([CH3:25])[C:20]=2[N+:22]([O-:24])=[O:23])[N:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 14797Potassium HydroxideHCID 39944183-Methyl-1,4-dinitropyrazoleHCID 178493561HCID 178493561, 화합물

생성물 1

HCID 178493560HCID 178493560, 화합물수율 78.5%

시약·촉매·용매 2

HCID 702Ethanol용매HCID 962Water용매

실험 절차

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

4,6-Dimethoxy-2-mercaptopyrimidine (4.65 g) was dissolved in water containing potassium hydroxide (1.7 g in 75 mls of water). 1,4-Dinitro-3-methylpyrazole (4.65 g) dissolved in the minimum of ethanol was then added dropwise. After the exothermic reaction had subsided, the mixture was stirred for 45 minutes. The precipitated solid was filtered off, washed with fresh water, and dried to give 6.3 g of the desired product, mp 175°-6° C.

후처리

  1. additionwas then added dropwise
  2. customAfter the exothermic reaction
  3. filtrationThe precipitated solid was filtered off
  4. washwashed with fresh water
  5. customdried

출처 및 근거

ORD 기록
ord-a71f3f4234544da0a7aace752bbf3d04
출처 데이터셋
uspto-grants-1996_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05559081

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