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Triethylamine → HCID 39235298、化合物

HRID 1360543
ノート
印刷プレビュー

反応式

HRID 1360543 の反応式
C(N(CC)CC)C.[OH:8][CH2:9][CH2:10][N:11]1[C:15]([CH3:16])=[CH:14][C:13]([C:17]([NH2:19])=O)=[N:12]1.FC(F)(F)C(OC(=O)C(F)(F)F)=O>ClCCl>[OH:8][CH2:9][CH2:10][N:11]1[C:15]([CH3:16])=[CH:14][C:13]([C:17]#[N:19])=[N:12]1
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 8471Triethylamine2 回HCID 9845Trifluoroacetic anhydride2 回HCID 669590521-(2-hydroxyethyl)-5-methyl-1H-pyrazole-3-carboxamide

生成物 1

HCID 39235298HCID 39235298、化合物収率 183.8%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

実験手順

Under a nitrogen atmosphere, triethylamine (17.9 g, 177 mmol) was added to a slurry of 1-(2-hydroxyethyl)-5-methyl-1H-pyrazole-3-carboxamide (7.0 g, 41.4 mmol) in dichloromethane (70 mL). The mixture was cooled in an ice bath and then a solution of trifluoroacetic anhydride (15.6 g, 74.2 mmol) in dichloromethane (70 mL) was added over a period of 10 minutes. All of the solids dissolved to provide a cloudy solution. After 1 hour additional triethylamine (70.6 mmol) was added and the reaction mixture was cooled in an ice bath. Trifluoroacetic anhydride (35.3 mmol) was added neat over a period of 5 minutes. The reaction mixture was stirred for 10 minutes then the ice bath was removed and the reaction mixture was stirred for 30 minutes. The reaction mixture was diluted with 2 M aqueous sodium carbonate (100 mL) and water (100 mL) then extracted with chloroform (×3). The extracts were combined, dried over magnesium sulfate, filtered, and concentrated under reduced pressure to provide 11.5 g of 1-(2-hydroxyethyl)-5-methyl-1H-pyrazole-3-carbonitrile a brown oil.

後処理

  1. temperatureThe mixture was cooled in an ice bath
  2. dissolutionAll of the solids dissolved
  3. customto provide a cloudy solution
  4. temperaturethe reaction mixture was cooled in an ice bath
  5. customthe ice bath was removed
  6. stirringthe reaction mixture was stirred for 30 minutes
  7. additionThe reaction mixture was diluted with 2 M aqueous sodium carbonate (100 mL) and water (100 mL)
  8. extractionthen extracted with chloroform (×3)
  9. dry with materialdried over magnesium sulfate
  10. filtrationfiltered
  11. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-bc0ed0adde914507b73cdc86e7c7e6ba
出典データセット
uspto-grants-2011_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07879849B2

反応ノート

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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