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Triethylamine → 1-(3-Fluorobenzoyl)pyrazolidin-3-one

HRID 1629972
ノート
印刷プレビュー

反応式

HRID 1629972 の反応式
[NH:1]1[CH2:5][CH2:4][C:3](=[O:6])[NH:2]1.[F:7][C:8]1[CH:9]=[C:10]([CH:14]=[CH:15][CH:16]=1)[C:11](O)=[O:12].C(N(CC)CC)C.CCCP1(OP(CCC)(=O)OP(CCC)(=O)O1)=O>ClCCl>[F:7][C:8]1[CH:9]=[C:10]([CH:14]=[CH:15][CH:16]=1)[C:11]([N:1]1[CH2:5][CH2:4][C:3](=[O:6])[NH:2]1)=[O:12]
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 8471TriethylamineHCID 99683-Fluorobenzoic AcidHCID 111923Propylphosphonic anhydrideHCID 1514973-Pyrazolidone

生成物 1

HCID 711848671-(3-Fluorobenzoyl)pyrazolidin-3-one収率 32,422.5%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

To a solution of pyrazolidin-3-one (6.9 gm, 0.080 mmol, 1 equiv.) in dry dichloromethane (70 ml), 3-fluorobenzoic acid (12.3 gm, 0.088 mmol, 1.1 equiv.), triethylamine (24.3 gm, 0.240 mmol, 3 equiv.) and 1-propane phosphonic acid cyclic anhydride (60% by weight in ethyl acetate) (51 gm, 0.16 mmol, 2 equiv.) were added in cooling condition and stirred for overnight at room temperature. The reaction mixture was concentrated and the residue was poured in water (500 ml), extracted with dichloromethane (100 ml×2) and concentrated. The crude product was purified by silica gel column using (60-120) mesh to get the pure product as yellow oil (5.4 gm, 32% yield).

後処理

  1. temperaturein cooling condition
  2. concentrationThe reaction mixture was concentrated
  3. additionthe residue was poured in water (500 ml)
  4. extractionextracted with dichloromethane (100 ml×2)
  5. concentrationconcentrated
  6. customThe crude product was purified by silica gel column

出典と根拠

ORDレコード
ord-3e10c8ac1cd74efbaed5448a27f5b0dc
出典データセット
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08791114B2

反応ノート

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