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Ethyl formate → HCID 178442218、化合物

HRID 721979
ノート
印刷プレビュー

反応式

HRID 721979 の反応式
C[O-].[Na+].[CH2:4]([CH:6]([CH2:10][CH3:11])[C:7](=O)[CH3:8])[CH3:5].[CH:12](OCC)=O.O.[NH2:18][NH2:19]>C(OCC)C>[CH2:4]([CH:6]([C:10]1[CH:11]=[CH:12][NH:19][N:18]=1)[CH2:7][CH3:8])[CH3:5]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 8025Ethyl formateHCID 24654Hydrazine hydrate (1:1)HCID 802242-Pentanone, 3-ethyl-HCID 10942334Sodium Methoxide

生成物 1

HCID 178442218HCID 178442218、化合物収率 67.9%

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒3 回

実験手順

To a stirred suspension of sodium methoxide (23.6 g, 0.437 mol) in diethyl ether (˜800 mL) was added dropwise a solution of 3-ethyl-2-pentanone (49.9 g, 0.437 mol) and ethyl formate (32.4 g, 0.437 mol) in diethyl ether (˜200 mL) at temperatures between 10° C. and 20° C. After the addition, the reaction mixture was allowed to warm up to room temperature, and stirred at room temperature for 2 hours. Additional diethyl ether (˜800 mL) was then added. The reaction mixture was stirred at room temperature for one additional hour and then concentrated. The residue was suspended in a solution of ethanol (950 mL) and acetic acid (30 mL). To this suspension was added hydrazine monohydrate (24 mL, 0.49 mol). The reaction mixture was heated at reflux for 60 hours and was then allowed to cool slowly to room temperature. The reaction mixture was then concentrated. To the residue was added 200 mL of 1N hydrochloric acid, followed by ˜75 mL of concentrated hydrochloric acid until pH ˜0. The acidic aqueous solution was then washed twice with diethyl ether (˜250 mL each). The pH of the aqueous solution was then adjusted to 9–10 by addition of aqueous 50% sodium hydroxide solution. The aqueous solution was then extracted twice with diethyl ether (˜300 mL each). The diethyl ether extracts were combined, dried over MgSO4 and concentrated to give the title compound as a pale yellow oil (41 g).

後処理

  1. additionAfter the addition
  2. stirringThe reaction mixture was stirred at room temperature for one additional hour
  3. concentrationconcentrated
  4. temperatureThe reaction mixture was heated
  5. temperatureat reflux for 60 hours
  6. temperatureto cool slowly to room temperature
  7. concentrationThe reaction mixture was then concentrated
  8. additionTo the residue was added 200 mL of 1N hydrochloric acid
  9. washThe acidic aqueous solution was then washed twice with diethyl ether (˜250 mL each)
  10. additionThe pH of the aqueous solution was then adjusted to 9–10 by addition of aqueous 50% sodium hydroxide solution
  11. extractionThe aqueous solution was then extracted twice with diethyl ether (˜300 mL each)
  12. dry with materialdried over MgSO4
  13. concentrationconcentrated

出典と根拠

ORDレコード
ord-9e912be8411f48ada935478033e7cb2f
出典データセット
uspto-grants-2006_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07138361B2

反応ノート

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