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Diisopropylethylamine → HCID 178469923、化合物

HRID 1753100
ノート
印刷プレビュー

反応式

HRID 1753100 の反応式
Cl.[NH2:2][NH2:3].CCN(C(C)C)C(C)C.C(O/[CH:16]=[C:17](/[C:23](=O)[C:24]([F:27])([F:26])[F:25])\[C:18]([O:20][CH2:21][CH3:22])=[O:19])C>C(O)C>[CH2:21]([O:20][C:18]([C:17]1[C:23]([C:24]([F:27])([F:26])[F:25])=[N:2][NH:3][CH:16]=1)=[O:19])[CH3:22]
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 81531DiisopropylethylamineHCID 115031Hydrazinium chlorideHCID 2737179Ethyl 2-(ethoxymethylene)-4,4,4-trifluoroacetoacetate

生成物 1

HCID 178469923HCID 178469923、化合物収率 46.8%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

To a suspension of hydrazine hydrochloride (10 g, 146.66 mmol) in ethanol (500 mL) at −20° C. was added DIPEA (45.3 mL, 266.66 mmol) followed by stirring at this temperature for 10 minutes. Ethyl (2Z)-2-(ethoxymethylene)-4,4,4-trifluoro-3-oxobutanoate (Preparation 113, 32 g, 133.33 mmol) was added and the reaction stirred at room temperature for 18 hours. The reaction was concentrated in vacuo and diluted with EtOAc. The organic solution was washed with water, dried over sodium sulphate and concentrated in vacuo. The residue was purified using silica gel column chromatography eluting with 30% EtOAc in hexane to afford the title compound (13 g) that was taken directly on to the next step.

後処理

  1. stirringthe reaction stirred at room temperature for 18 hours
  2. concentrationThe reaction was concentrated in vacuo
  3. additiondiluted with EtOAc
  4. washThe organic solution was washed with water
  5. dry with materialdried over sodium sulphate
  6. concentrationconcentrated in vacuo
  7. customThe residue was purified
  8. washeluting with 30% EtOAc in hexane

出典と根拠

ORDレコード
ord-3563c8f4a88e4bf4ac0c080521875824
出典データセット
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09163021B2

反応ノート

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