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Ethyl Acetate → HCID 15117198、化合物

HRID 1029605
ノート
印刷プレビュー

反応式

HRID 1029605 の反応式
[CH2:1]([O:4][C:5]([N:7]1[CH2:11][CH2:10][CH2:9][C@H:8]1[C:12]([OH:14])=O)=[O:6])[CH:2]=[CH2:3].[CH:15]1(N=C=NC2CCCCC2)CCCCC1.CC1(C)OC(=O)CC(=O)O1.C(OCC)(=O)C>ClCCl.CN(C)C1C=CN=CC=1>[C:12]([C@@H:8]1[CH2:9][CH2:10][CH2:11][N:7]1[C:5]([O:4][CH2:1][CH:2]=[CH2:3])=[O:6])(=[O:14])[CH3:15]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 8857Ethyl AcetateHCID 10868DicyclohexylcarbodiimideHCID 162492,2-Dimethyl-1,3-dioxane-4,6-dioneHCID 109434831-(2-Propen-1-yl) (2S)-1,2-pyrrolidinedicarboxylate

生成物 1

HCID 15117198HCID 15117198、化合物収率 43.8%

試薬・触媒・溶媒 2

HCID 14284
4-(Dimethylamino)pyridine
触媒
HCID 6344Dichloromethane溶媒

実験手順

To a solution of (2S)-1-allyloxycarbonyl-2-carboxypyrrolidine (10 g) in dichloromethane (100 ml) were added dicyclohexylcarbodiimide (9.8 g), Meldrum's acid (6.8 g) and 4-dimethylaminopyridine (5.8 g) at 0° C. After stirring for 24 hours at ambient temperature, the resulting precipitate was removed by filtration. The filtrate was washed with 1N hydrochloric acid solution, evaporated in vacuo. The residue was dissolved in a mixture of acetic acid (80 ml) and water (60 ml), and refluxed for 1 hour. Evaporation of the solvent gave a residue, which was taken up into ethyl acetate. The solution was washed in turn with saturated sodium bicarbonate and brine, dried over magnesium sulfate, and evaporated. The residue was chromatographed on silica gel eluting with a mixture of n-hexane and ethyl acetate (2:1, V/V) to give (2S)-2-acetyl-1-allyloxycarbonylpyrrolidine (4.1 g).

後処理

  1. customthe resulting precipitate was removed by filtration
  2. washThe filtrate was washed with 1N hydrochloric acid solution
  3. customevaporated in vacuo
  4. dissolutionThe residue was dissolved in a mixture of acetic acid (80 ml) and water (60 ml)
  5. temperaturerefluxed for 1 hour
  6. customEvaporation of the solvent
  7. customgave a residue, which
  8. washThe solution was washed in turn with saturated sodium bicarbonate and brine
  9. dry with materialdried over magnesium sulfate
  10. customevaporated
  11. customThe residue was chromatographed on silica gel eluting with a mixture of n-hexane and ethyl acetate (2:1, V/V)

出典と根拠

ORDレコード
ord-88a95ca4f75f4efb945f07a2225c7d7d
出典データセット
uspto-grants-1992_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05102877

反応ノート

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