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Nitric Acid → HCID 178434486、化合物

HRID 2398617
ノート
印刷プレビュー

反応式

HRID 2398617 の反応式
Br[C:2]1[C:3]([CH3:8])=[N:4][NH:5][C:6]=1[Br:7].[N+:9]([O-])([OH:11])=[O:10].O>S(=O)(=O)(O)O>[Br:7][C:6]1[NH:5][N:4]=[C:3]([CH3:8])[C:2]=1[N+:9]([O-:11])=[O:10]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 944Nitric AcidHCID 962WaterHCID 178434484HCID 178434484、化合物

生成物 1

HCID 178434486HCID 178434486、化合物

試薬・触媒・溶媒 1

HCID 1118Sulfuric Acid溶媒

反応条件

温度
9 °C

実験手順

6.5 g (0.027 mole) of 4,5-dibromo-3-methylpyrazole was dissolved in 20 ml of concentrated sulfuric acid. The solution was cooled to 9° C. and 10 ml of 90% nitric acid was added dropwise. The solution was stirred 30 minutes and then slowly heated to 60° C. and kept at that temperature for 30 minutes. The solution was cooled and poured into water. The mixture was extracted with ether and the ether was washed with water. The ether solution, after drying over magnesium sulfate was concentrated in vacuo and gave a white solid (1.5 g). One recrystallization from ethyl acetate gave a solid product.

後処理

  1. temperatureslowly heated to 60° C.
  2. waitkept at that temperature for 30 minutes
  3. temperatureThe solution was cooled
  4. extractionThe mixture was extracted with ether
  5. washthe ether was washed with water
  6. dry with materialThe ether solution, after drying over magnesium sulfate
  7. concentrationwas concentrated in vacuo

出典と根拠

ORDレコード
ord-4e336a0aba884b64a848a83567d9f284
出典データセット
uspto-grants-1977_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04025530

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート