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Acetic Anhydride → N-(5-methyl-1H-pyrazol-3-yl)acetamide

HRID 1953802
ノート
印刷プレビュー

反応式

HRID 1953802 の反応式
C(=O)(O)[O-].[Na+].[NH2:6][C:7]1[CH:11]=[C:10]([CH3:12])[NH:9][N:8]=1.[C:13](OC(=O)C)(=[O:15])[CH3:14]>O>[C:13]([NH:6][C:7]1[CH:11]=[C:10]([CH3:12])[NH:9][N:8]=1)(=[O:15])[CH3:14]
参加物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 7918Acetic AnhydrideHCID 931461H-Pyrazol-3-amine, 5-methyl-HCID 516892Sodium Bicarbonate

生成物 1

HCID 5246311N-(5-methyl-1H-pyrazol-3-yl)acetamide収率 59.6%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

50.4 g (0.6 mol) of sodium bicarbonate were added in small amounts at room temperature to a solution of 19.4 g (0.2 mol) of 3-amino-5-methyl-1H-pyrazole in 200 cm3 of water. 37.8 cm3 (0.4 mol) of acetic anhydride were added dropwise to this solution and then the mixture was heated at reflux for 2 hours. The solution was subsequently brought back to room temperature, a white solid crystallized and was pulled dry on sintered glass and then washed with 100 cm3 of water. After drying under vacuum at 40° C., 16.6 g of the expected product were obtained in the form of pearlescent-white crystals, the melting point of which was between 210° C. and 212° C.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. temperaturethe mixture was heated
  2. temperatureat reflux for 2 hours
  3. customwas subsequently brought back to room temperature
  4. customa white solid crystallized
  5. customwas pulled dry on sintered glass
  6. washwashed with 100 cm3 of water
  7. customAfter drying under vacuum at 40° C.

出典と根拠

ORDレコード
ord-e6217960ed134687af208f44f197710d
出典データセット
uspto-grants-2000_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06118008

反応ノート

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